Pyrrolo [2,3-D] pyrimidines as non-nucleoside reverse transcriptase inhibitors for treatment of HIV

ABSTRACT

This application concerns certain 2-phenylamino-6-aryl amino-, 6-aryloxy-, and 6-arylthio-purines, -azapurines and -deazapurines. These compounds are non-nucleoside reverse transcriptase inhibitors and have potential as anti-HIV treatment.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional patent application of U.S. application Ser. No. 11/919,786, filed Jan. 14, 2009, now U.S. Pat. No. 8,227,601 entitled “DIARYL-PURINES, -AZAPURINES AND -DEAZAPURINES AS NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS FOR TREATMENT OF HIV”, which is the national stage entry of PCT/US06/17677, filed May, 5, 2006, which claims priority to U.S. Provisional Application Ser. No. 60/678,667, filed May 5, 2005, all of which applications are incorporated herein by reference in their entirety.

FIELD OF THE INVENTION

This application concerns certain 2-phenylamino-6-aryl amino-, 6-aryloxy-, and 6-arylthio-purines, -azapurines and -deazapurines. These compounds are non-nucleoside reverse transcriptase inhibitors and have potential as anti-HIV treatment.

BACKGROUND OF THE INVENTION

Human Immunodeficiency Virus (HIV) presents a public-health and social catastrophe too well known to require documentation. One therapeutic approach to HIV has been inhibition of the viral RNA-dependent RNA polymerase; this enzyme is frequently referred to as “reverse transcriptase,” abbreviated “RT.” The first RT inhibitors were nucleoside analogs such as AZT and dd. Although such nucleoside RT inhibitors were frequently effective against the wild-type virus, any single-drug treatment has been hobbled by the virus's ability to readily produce drug-resistant mutants. This has led to an intense search for non-nucleoside RT inhibitors (“NNRTIs”) which are both effective and capable of retaining their effectiveness despite drug-resistance mutations. A recent review of NNRTIs can be found Balzarni, J., 2004, Cur. Top. Med. Chem. 4, 921-44 (Erratum ibid. 4, 1825).

Four leading NNRTI are: 1) Efavirenz (4S)-6-chloro-4-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one; 2) Capravirine: 1H-Imidazole-2-methanol, 5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-1-(4-pyridinylmethyl)-carbamate (ester); 3) Etravirine (TMC 125): 4-((6-amino-5-bromo-2-((4-cyanophenyl)amino)-4-pyrimidinyl)oxy)-3,5-dimethyl-benzonitrile; and 4) Rilpivirine (TMC-278): 4-([4-[(4-[(1E)-2-cyanoethenyl]-2,6-dimethylphenyl)amino]-2-pyrimidinyl)amino]benzonitrile. Rilpivirine and Etravirine belong to a subclass of NNRTIs called diarylpyrmidines (“DAPY”). For a review of these DAPY NNRTIs see Ludovici, D. W., et al., 2002, Bioorg. Med. Chem. Lett. 11, 2235-9. An extensive patent literature also exists for DAPY. U.S. Pat. No. 6,197,779; WO 00/27850; WO 2003/016306; and WO 2004/069812, all assigned to Janssen Pharmaceuticals.

Diaryl compounds similar to Etravirine and Rilpivirine where the pyrimidine moiety is replaced by a purine are described in WO 2005/028479, which also is assigned to Janssen.

BRIEF DESCRIPTION OF THE INVENTION

The invention provides a compound of formula I

where the dashed line represents a double bond that may be located either between A and B or between B and D, where A is —N═, N(Z) or C(Z); B is CH or ═N—; D is CW or ═N—, or N(W); T is NH, O or S; Z is H, F, Cl, Br, CH₃, CH₂CH₃, cyclopropyl, or benzyl, in which the phenyl moiety of the benzyl group is optionally substituted with methyl or methoxy, provided that Z is not F or Cl when A is NZ; W is H, F, Cl, Br, methyl, ethyl, cyclopropyl, allyl, CH₂CF₃, cyanomethyl, cyanoethyl, CH═CHCN, or benzyl, in which the phenyl moiety of the benzyl group is optionally substituted with one or two groups selected independently from methoxy and methyl, provided that W is not F or Cl when D is NW; V is F, Cl, CN, SO₂CH₃, SO₂NH₂, SO₂NHCH₃, C≡CCH₃, or CH═CHCN; provided that when D is CW, A is not CZ and further provided that when neither A nor D is CZ or CW, then B is CH; and Ar is selected from (a), (b), (c), and (d) below:

wherein each R^(P) is selected from among methyl, ethyl, propyl, isopropyl, cyclopropylmethyl, or C₃-C₆ cycloalkyl, cyano, CH═CHCN, Cl, Br, I, acetyl and alkylamino; R⁴, R⁵, and each R⁶ are independently selected from among H, F, Cl, Br, CH₃, CF₃, CH₂F, CHF₂, isopropyl, cyclopropyl, OCH₃, OH, OCF₃, NH₂ and NHCH₃, or R⁶ and R^(p) on adjacent ring atoms, together with the ring atoms to which they are attached, form an additional fused five-membered ring; Q and Q′ are independently selected from N and CH; R⁷ is Cl, Br, I, CH₃, CF₃, OCH₃, isopropyl, cyclopropyl, t-butyl, or cyclobutyl; and R⁸-R¹¹ are, independently, H or CH₃.

Compounds of formula I have inhibitory activity against both wild-type and mutated forms of human immunodeficiency virus type 1 (HIV-1).

DETAILED DESCRIPTION OF THE INVENTION

In one embodiment this invention provides a compound of formula IA, in which the 6-linker T of formula I is T′, which may be O or S.

When T of formula I or T′ of formula IA is O, the invention excludes 1) compounds where both R^(p) and V are CH═CHCN or cyano unless at least one of A or D is neither —N═ nor —NH— and 2) compounds where a) R is CH═CHCN, cyano, or methyl; b) V is cyano or CH═CHCN; and c) A and D are both one of —N═; N-benzyl or N-(substituted benzyl).

In one subgeneric embodiment, the invention provides a compound of formula IA where Ar is selected from 4-cyclopropyl phenyl; 4-cyclopropylmethyl phenyl; 4-bromophenyl; 4-cyclopropyl-naphth-1-yl; 2,6-dimethyl-4-cyanophenyl; 2,6-dimethoxy-4-cyanophenyl; 2,6-dimethyl-4-(2-cyanoethenyl)phenyl; 2,6-dimethoxy-4-(2-cyanoethenyl)phenyl; 2-methyl-4-cyclopropyl phenyl; 2,6-dimethyl-4-cyclopropyl phenyl; 2,6-di-trifluoromethyl-4-cyclopropyl phenyl; 2,4,6-trimethyl phenyl; and 2,6-dimethyl-4-acetyl phenyl.

In another subgeneric embodiment, the invention contemplates a compound of formula IA where Ar is selected from the following: 5-cyclopropyl-8-quinolyl; 5-isopropyl-8-quinolyl; 5-cyano-8-quinolyl; 5-cyclopropyl-7-trifluoromethyl-8-quinolyl; 5-acetyl-8-quinolyl; 5-cyano-7-methoxy-8-quinolyl; 5-cyano-7-methyl-8-quinolyl; 5-cyclopropyl-7-trifluoromethoxy-8-isoquinolyl; 5-cyano-8-isoquinolyl; 5-cyano-7-methoxy-8-isoquinolyl; 5-cyano-7-methyl-8-isoquinolyl; 5-cyclobutyl-7-difluoromethyl-8-isoquinolyl; 5,7-dimethyl-8-cinnolyl; 5-cyclopropyl-7-methyl-8-cinnolyl; and 5-(2-cyanoethenyl)-7-methyl-8-cinnolyl.

In another subgeneric embodiment, the invention provides a compound of formula IA-1

where Ar, V, W, and Z are defined as for formula I.

In another subgeneric embodiment, the invention provides a compound of formula IA-2

where Ar, V, W, and Z are defined as for formula I.

In another subgeneric embodiment, the invention provides a compound of formula IA-3

where Ar, V, W, and Z are defined as for formula I.

In another subgeneric embodiment, this invention provides a compound of formula IA-4

where Ar, V, W, and Z are defined as for formula I.

In another subgeneric embodiment, this invention provides a compound of formula IA-5

where Ar, V, W, and Z are defined as for formula I.

In another subgeneric embodiment, this invention provides a compound of formula IA-6

where Ar, V, W, and Z are defined as for formula I.

In another subgeneric embodiment, this invention provides a compound of formula IA-7

where Ar, V, W, and Z are defined as for formula I.

In another subgeneric embodiment, this invention provides a compound of formula IA-8

where Ar, V, W, and Z are defined as for formula I.

In another subgeneric embodiment, this invention provides a compound of formula IA-9

where Ar, V, W, and Z are defined as for formula I.

In another subgeneric embodiment, this invention provides a compound of formula IA-10

where Ar, V, W, and Z are defined as for formula I.

In another embodiment, this invention provides a compound of formula IB

where all substituents are as described above, except that when Ar is (c), this invention excludes compounds in which V is either cyano or CH═CHCN, unless A or D is CZ or CW.

In one subgeneric embodiment, the invention provides a compound of formula IB where Ar is (c), subject to the exclusion in the immediately preceding paragraph.

In a more specific subgeneric embodiment, the invention provides a compound of formula IB where Ar is

where R^(p) is CN, CH═CHCN, or cyclopropyl; where R⁶ and R⁷ are either both methyl or both methoxy; and subject to the exclusion described above for formula IB.

In another subgeneric embodiment, this invention provides a compound of formula IB-1.

In another subgeneric embodiment, this invention provides a compound of formula IB-2.

where Ar, V, W, and Z are as described above for formula IB.

In another subgeneric embodiment, the invention provides a compound of formula IB-3.

where Ar, W, and Z are as described above for formula IB.

In another subgeneric embodiment, the invention provides a compound of formula IB-4.

where Ar, V, and Z are as described above for formula IB.

In more specific embodiments, the invention provides compounds of any of IA-1, IA-2, IA-3, IA-4, IA-5, IA-6, IA-7, IA-8, IA-9, IA-10, IB-1, IB-2, IB-3, and IB-4, where Ar is (a).

In additional more specific embodiments, the invention provides compounds of any of IA-1, IA-2, IA-3, IA-4, IA-5, IA-6, IA-7, IA-8, IA-9, IA-10, IB-1, IB-2, IB-3, and IB-4, where Ar is (b).

In additional more specific embodiments, the invention provides compounds of any of IA-1, IA-2, IA-3, IA-4, IA-5, IA-6, IA-7, IA-8, IA-9, IA-10, IB-1, IB-2, IB-3, and IB-4, where Ar is (c).

In additional more specific embodiments, the invention provides compounds of any of IA-1, IA-2, IA-3, IA-4, IA-5, IA-6, IA-7, IA-8, IA-9, IA-10, IB-1, IB-2, IB-3, and IB-4, where Ar is (d).

In a more specific subgeneric embodiment, this invention provides or contemplates a compound of formula IA-7, IA-8, IA-9, or IA-10, where Ar is 4-cyclopropyl-, 4-acetyl-, 4-methyl-, 4-bromo-, or 4-cyano-2,6-di-substituted phenyl.

In another more specific subgeneric embodiment, this invention provides or contemplates a compound of formula IA-1, IA-2, IA-3, or IA-4, where Ar is 4-cyclopropyl-, 4-acetyl-, 4-methyl-, 4-bromo-, or 4-cyano-2,6-di-substituted phenyl.

In another more specific subgeneric embodiment, this invention provides or contemplates a compound of formula IA-5 or IA-6, where Ar is 4-cyclopropyl-, 4-acetyl-, 4-methyl-, 4-bromo- or 4-cyano-2,6-di-substituted phenyl.

Synthetic Procedures

Compounds of this invention which are of the 7-deaza-8-azapurine type can be prepared according to Scheme 1.

Compound (1), 2-mercapto-6-hydroxy-7-deaza-8-aza-purine, can be synthesized by published procedures known to those skilled in the art. Youssif, S., et al., 2003, Bull. Kor. Chem. Soc., 24, 1429-32; Bontems, R. J., et al., 1990, J. Med. Chem. 33, 2174-8; Badger, G. M., & Rao, R. P., 1965, Aust. J. Chem. 18, 1267-71.

Alternatively, the 7-deaza-8-azapurines can be synthesized according to Scheme 2, where “PMBCl” is p-methoxy benzyl chloride. The starting material is prepared by published procedures known to those skilled in the art. Seela, F., 1999, Helv. Chim. Act. 82, 105-124; Taylor, E., 1992, Tetrahedron 48, 8089-100; Seela, F., 1986, Helv. Chim. Act. 69, 1602-1613.

The 8-aza-9-deazapurines of this invention can be synthesized according to Scheme 3. The synthesis of the starting material was described by Lewis, A. F., & Townsend, L. B., 1982, J. Am. Chem. Soc. 104, 1073-78.

The 9-deazapurines of this invention can be synthesized by Scheme 4. The synthesis of the starting material is described by Kielich, Klaus, ed., “Synthetic Communications” 2002 vol. 32, pp-3797-3802.

The 7-deazapurines of this invention are prepared by the procedure of Scheme 5. The starting material can be synthesized by the condensation of 2,6-diamino-1,2-dihydro[3H]pyrimidin-4-one with chloroacetaldehyde followed by treatment with phosphorus oxychloride, as indicated in Examples 1 and 3.

The purine compounds of this invention can be synthesized by strategies similar to those provided above, using N⁷-benzyl-2,6-dichloropurine as the starting material. This procedure is illustrated in WO 2005/028479.

Example 1

Step AI

2-Amino-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one

To a mixture of 2,4-diamino-6-hydroxypyrimidine (20.0 g, 159 mmol) and NaOAc (26.0 g, 317 mmol) in H₂O (300 mL) at 65° C. was added a solution of chloroacetaldehyde (22.0 mL, 50% in H₂O, 173 mmol) in H₂O (22 mL) dropwise for 90 min. The mixture was stirred at 65° C. for an additional 2 h and cooled to room temperature. The reaction mixture was concentrated in vacuo to one third of its original volume and stored at 4° C. for 16 h. The light pink precipitates were filtered, washed with an ice cold H₂O (5 mL), and dried under high vacuum for 16 h. The precipitates were placed in Soxhlet extractor and refluxed with methanol (200 mL) for 24 h. The methanol was concentrated to give 13.3 g (56%) of 2-amino-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one as a light pink solid.

Step A2

4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine

To a solution of 2-amino-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one (5.00 g, 33.3 mmol), dimethylaniline (4.22 mL, 41.0 mmol) and benzyltriethylammonium chloride (15.2 g, 66.6 mmol) in acetonitrile (25 mL) at room temperature under argon was added POCl₃ (18.6 mL, 200 mmol) dropwise for 30 min. The mixture was refluxed at 85° C. for 3 h and cooled to room temperature. The reaction was concentrated in vacuo to brown oil and to the oil was added an ice cold H₂O (10 mL). The pH of the solution was adjusted to 5 by the addition of an aqueous NH₄OH solution. Silica gel chromatography (CH₂Cl₂:MeOH=95:5) yielded 2.53 g (45%) of 4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine as a light yellow solid. The product was then benzylated at N⁷ using standard techniques.

Step C

7-benzyl-4-(2,4,6-trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine

To a solution of 2,4,6-trimethylphenol (161 mg, 1.16 mmol) in 1-methyl-2-pyrridone (2 mL) in a sealed tube was added NaH (46 mg, 1.16 mmol). The reaction mixture was stirred at room temperature for 15 min and a solution of 7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (100 mg, 0.39 mmol) in 1-methyl-2-pyrridone (1 mL) was added to the mixture. The mixture was heated at 150° C. for 16 h and cooled to room temperature. The reaction mixture was poured into ice water and extracted with EtOAc (2×20 mL). The combined organic solution was washed with H₂O (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 107 mg (77%) of 7-benzyl-4-(2,4,6-trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine.

Step D

7-benzyl-2-fluoro-4-(2,4,6-trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidine

To 7-benzyl-4-(2,4,6-trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (105 mg, 0.29 mmol) in a polyethylene flask at −50° C. under argon was added 60% HF in pyridine (12 mL). To the resulting solution tert-butylnitrite (0.052 mL, 0.44 mmol) was added dropwise for 5 min. The reaction was warmed to −40° C. and stirred for 30 min at the temperature. The reaction mixture was diluted with CHCl₃ (100 mL) and poured into K₂CO₃ (3 g) in a beaker. Ice water (50 mL) was carefully added to the mixture. The CHCl₃ layer was separated, washed with aqueous NaHCO₃ solution (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 72 mg (68%) of 7-benzyl-2-fluoro-4-(2,4,6-trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidine as a light yellow solid.

Step E

4-[7-benzyl-4-(2,4,6-trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile

To a solution of 4-aminobenzonitrile (101 mg, 0.86 mmol) in 1-methyl-2-pyrridone (1 mL) was added NaH (34 mg, 0.86 mmol). The reaction mixture was stirred at room temperature for 15 min and a solution of 7-benzyl-2-fluoro-4-(2,4,6-trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidine (62 mg, 0.17 mmol) in 1-methyl-2-pyrridone (1 mL) was added to the mixture. The mixture was stirred at room temperature for 1 h, poured into ice water, and extracted with EtOAc (2×20 mL). The combined organic solution was washed with H₂O (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 64 mg (82%) of 4-[7-benzyl-4-(2,4,6-trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile.

Step F

4-[4-(2,4,6-Trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile

To a solution of 4-[7-benzyl-4-(2,4,6-trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile (38 mg, 0.083 mmol) in 1,2-dichlorobenzene (1 mL) was added aluminum chloride (55 mg, 0.42 mmol). The reaction mixture was stirred at 160° C. for 4 h and cooled to room temperature. The mixture was poured into ice water and extracted with CH₂Cl₂ (2×10 mL). The combined organic solution was washed with brine (10 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=50:50) yielded 15 mg (49%) of 4-[4-(2,4,6-trimethyl-phenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile as a tan solid.

Example 2

Step A

7-benzyl-4-(2,4,6-trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine

To a solution of 2,4,6-trimethylbenzene-1-thiol (231 mg, 1.52 mmol) in 1-methyl-2-pyrridone (2 mL) was added NaH (58 mg, 1.52 mmol). The reaction mixture was stirred at room temperature for 15 min and a solution of 7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (131 mg, 0.51 mmol) in 1-methyl-2-pyrridone (2 mL) was added to the mixture. The mixture was heated at 60° C. for 16 h and cooled to room temperature. The reaction was poured into ice water and extracted with EtOAc (2×20 mL). The combined organic solution was washed with H₂O (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 180 mg (94%) of 7-benzyl-4-(2,4,6-trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine.

Step B

7-benzyl-2-fluoro-4-(2,4,6-trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidine

To 7-benzyl-4-(2,4,6-trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (155 mg, 0.41 mmol) in a polyethylene flask at −50° C. under argon was added 60% HF in pyridine (12 mL). To the solution was added tert-butylnitrite (0.074 mL, 0.62 mmol) dropwise for 5 min. The reaction was warmed to −40° C. and stirred for 30 min at the temperature. The reaction was diluted with CHCl₃ (100 mL) and poured into K₂CO₃ (3 g) in a beaker. To the mixture was carefully added ice water (50 mL). The CHCl₃ layer was separated, washed with aqueous NaHCO₃ solution (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 118 mg (77%) of 7-benzyl-2-fluoro-4-(2,4,6-trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidine as a yellow solid.

Step C

4-[7-benzyl-4-(2,4,6-trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile

To a solution of 4-aminobenzonitrile (184 mg, 1.56 mmol) in 1-methyl-2-pyrridone (2 mL) was added NaH (62 mg, 1.56 mmol). The reaction mixture was stirred at room temperature for 15 min and a solution of 7-benzyl-2-fluoro-4-(2,4,6-trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidine (118 mg, 0.31 mmol) in 1-methyl-2-pyrridone (2 mL) was added to the mixture. The mixture was stirred at room temperature for 4 h, then poured into ice water and extracted with EtOAc (2×20 mL). The combined organic solution was washed with H₂O (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 123 mg (83%) of 4-[7-benzyl-4-(2,4,6-trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile.

Step D

4-[4-(2,4,6-Trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile

To a solution of 4-[7-benzyl-4-(2,4,6-trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile (103 mg, 0.21 mmol) in 1,2-dichlorobenzene (2 mL) was added aluminum chloride (87 mg, 0.65 mmol). The reaction mixture was stirred at 160° C. for 1.5 h and cooled to room temperature. The mixture was poured into ice water and extracted with CH₂Cl₂ (2×10 mL). The combined organic solution was washed with brine (10 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=50:50) yielded 28 mg (34%) of 4-[4-(2,4,6-trimethyl-phenylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile as a tan solid.

Example 3

Steps A and B as in Example 1 Step C

4-(2-Amino-7-benzyl-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile

To a solution of 4-hydroxy-3,5-dimethylbenzonitrile (1.62 mg, 11.0 mmol) in 1-methyl-2-pyrridone (5 mL) in a sealed tube was added NaH (441 mg, 11.0 mmol). The reaction mixture was stirred at room temperature for 15 min and a solution of 7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (950 mg, 3.67 mmol) in 1-methyl-2-pyrridone (5 mL) was added to the mixture. The mixture was heated at 150° C. for 16 h and cooled to room temperature. The reaction was poured into ice water and extracted with EtOAc (2×50 mL). The combined organic solution was washed with H₂O (50 mL) and brine (50 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 1.12 mg (83%) of 4-(2-amino-7-benzyl-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile.

Step D

4-(7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile

To 4-(2-amino-7-benzyl-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile (70 mg, 0.19 mmol) in a polyethylene flask at −50° C. under argon was added 60% HF in pyridine (12 mL). To the solution was added tert-butylnitrite (0.068 mL, 0.57 mmol) dropwise for 5 min. The reaction was warmed to −40° C. and stirred for 30 min at the temperature. The reaction was diluted with CHCl₃ (100 mL) and poured into K₂CO₃ (3 g) in a beaker. To the mixture was carefully added ice water (50 mL). The CHCl₃ layer was separated, washed with aqueous NaHCO₃ solution (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 36 mg (51%) of 4-(7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile.

Step E

4-[7-benzyl-2-(4-cyano-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile

To a solution of 4-aminobenzonitrile (54 mg, 0.46 mmol) in 1-methyl-2-pyrridone (1 mL) was added NaH (18 mg, 0.46 mmol). The reaction mixture was stirred at room temperature for 15 min and a solution of 4-(7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile (34 mg, 0.091 mmol) in 1-methyl-2-pyrridone (1 mL) was added to the mixture. The mixture was stirred at room temperature for 1 h, poured into ice water, and extracted with EtOAc (2×20 mL). The combined organic solution was washed with H₂O (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 28 mg (65%) of 4-[7-benzyl-2-(4-cyano-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile.

Step F

4-[2-(4-Cyano-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile

To a solution of 4-[7-benzyl-2-(4-cyano-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile (28 mg, 0.060 mmol) in 1,2-dichlorobenzene (1 mL) was added aluminum chloride (40 mg, 0.30 mmol). The reaction mixture was stirred at 160° C. for 45 min and cooled to room temperature. The mixture was poured into ice water and extracted with CH₂Cl₂ (2×10 mL). The combined organic solution was washed with brine (10 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=50:50) yielded 6 mg (27%) of 4-[2-(4-cyano-phenylamino)-71′-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile as a tan solid.

Example 4

Step A

7-benzyl-N4-(2,4,6-trimethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamine

To a suspension of 7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (200 mg, 0.78 mmol) and 2,4,6-trimethylaniline (0.44 mL, 3.08 mmol) in 2,2,2-trifluoroethanol (4 mL) was added trifluoroacetic acid (0.48 mL, 6.24 mmol). The resulting solution was heated at 100° C. for 2 days and cooled to room temperature. The reaction was concentrated to brown oil and diluted with CH₂Cl₂ (30 mL). The organic solution was washed with aqueous NaHCO₃ solution (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (CH₂Cl₂:MeOH=95:5) yielded 251 mg (90%) of 7-benzyl-N4-(2,4,6-trimethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamine.

Step B

(7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-(2,4,6-trimethyl-phenyl)-amine

To 7-benzyl-N4-(2,4,6-trimethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamine (251 mg, 0.70 mmol) in a polyethylene flask at −50° C. under argon was added 60% HF in pyridine (24 mL). To the solution was added tert-butylnitrite (0.42 mL, 3.5 mmol) dropwise for 10 min. The reaction was warmed to −40° C. and stirred for 30 min at the temperature. The reaction was diluted with CHCl₃ (200 mL) and poured into K₂CO₃ (6 g) in a beaker. To the mixture was carefully added ice water (100 mL). The CHCl₃ layer was separated, washed with aqueous NaHCO₃ solution (40 mL) and brine (40 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 56 mg (22%) of (7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-(2,4,6-trimethyl-phenyl)-amine.

Step C

4-[7-benzyl-4-(2,4,6-trimethyl-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile

To a suspension of (7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-(2,4,6-trimethyl-phenyl)-amine (42 mg, 0.12 mmol) and 4-aminobenzonitrile (55 mg, 0.47 mmol) in 2,2,2-trifluoroethanol (4 mL) was added trifluoroacetic acid (0.072 mL, 0.94 mmol). The resulting solution was heated at 90° C. for 16 h, then cooled to room temperature. The reaction was concentrated to produce a brown oil and diluted with CH₂Cl₂ (30 mL). The organic solution was washed with H₂O (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 34 mg (64%) of 4-[7-benzyl-4-(2,4,6-trimethyl-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile.

Step D

4-[4-(2,4,6-Trimethyl-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile

To a solution of 4-[7-benzyl-4-(2,4,6-trimethyl-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile (34 mg, 0.074 mmol) in 1,2-dichlorobenzene (1 mL) was added aluminum chloride (50 mg, 0.37 mmol). The reaction mixture was stirred at 160° C. for 2 h and cooled to room temperature. The mixture was poured into ice water and extracted with CHCl₃ (2×10 mL). The combined organic solution was washed with brine (10 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (CH₂Cl₂:Acetone=90:10) yielded 5 mg (19%) of 4-[4-(2,4,6-trimethyl-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-benzonitrile as a tan solid.

Example 5

Step A

4-(2-Amino-7-benzyl-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile

To a solution of 4-hydroxy-3,5-dimethylbenzonitrile (1.62 mg, 11.0 mmol) in 1-methyl-2-pyrridone (5 mL) in a sealed tube was added NaH (441 mg, 11.0 mmol). The reaction mixture was stirred at room temperature for 15 min and a solution of 7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (950 mg, 3.67 mmol) in 1-methyl-2-pyrridone (5 mL) was added to the mixture. The mixture was heated at 150° C. for 16 h and cooled to room temperature. The reaction was poured into ice water and extracted with EtOAc (2×50 mL). The combined organic solution was washed with H₂O (50 mL) and brine (50 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 1.12 mg (83%) of 4-(2-amino-7-benzyl-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile.

Step B

4-(7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile

To 4-(2-amino-7-benzyl-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile (70 mg, 0.19 mmol) in a polyethylene flask at −50° C. under argon was added 60% HF in pyridine (12 mL). To the solution was added tert-butylnitrite (0.068 mL, 0.57 mmol) dropwise for 5 min. The reaction was warmed to −40° C. and stirred for 30 min at the temperature. The reaction was then diluted with CHCl₃ (100 mL) and poured into K₂CO₃ (3 g) in a beaker. Ice water (50 mL) was carefully added. The CHCl₃ layer was separated, washed with aqueous NaHCO₃ solution (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 36 mg (51%) of 4-(7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile.

Step C

4-[7-benzyl-2-(4-cyano-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile

To a solution of 4-aminobenzonitrile (54 mg, 0.46 mmol) in 1-methyl-2-pyrridone (1 mL) was added NaH (18 mg, 0.46 mmol). The reaction mixture was stirred at room temperature for 15 min and a solution of 4-(7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile (34 mg, 0.091 mmol) in 1-methyl-2-pyrridone (1 mL) was added to the mixture. The mixture was stirred at room temperature for 1 h, poured into ice water and extracted with EtOAc (2×20 mL). The combined organic solution was washed with H₂O (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 28 mg (65%) of 4-[7-benzyl-2-(4-cyano-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile.

Step D

4-[2-(4-Cyano-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile

To a solution of 4-[7-benzyl-2-(4-cyano-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile (28 mg, 0.060 mmol) in 1,2-dichlorobenzene (1 mL) was added aluminum chloride (40 mg, 0.30 mmol). The reaction mixture was stirred at 160° C. for 45 min and cooled to room temperature. The mixture was poured into ice water and extracted with CH₂Cl₂ (2×10 mL). The combined organic solution was washed with brine (10 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=50:50) yielded 6 mg (27%) of 4-[2-(4-cyano-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile as a tan solid.

Example 6

4-Cyclopropyl-2,6-dimethylphenol

To a suspension of (4-bromo-2,6-dimethylphenoxy) tert-butyldimethylsilane (668 mg, 2.12 mmol) and tetrakis(triphenylphosphine)palladium (122 mg, 0.11 mmol) in THF (20 mL) was added cyclopropyl zinc chloride (28.0 mL, 11.2 mmol). The mixture was heated at 80° C. for 24 h and cooled to room temperature. The reaction was passed through a short pad of SiO₂ to remove the catalyst and the solution was concentrated to oil. The resulting oil was diluted in EtOAc (100 mL), washed with brine (100 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=90:10) yielded 370 mg (63%) of tert-butyl(4-cyclopropyl-2,6-dimethylphenoxy)dimethylsilane. To tert-butyl(4-cyclopropyl-2,6-dimethylphenoxy)dimethylsilane (320 mg, 1.16 mmol) in THF (10 mL) was added a solution of tetrabutylammonium fluoride (5.0 mL, 1 M in THF, 5.0 mmol) and acetic acid (0.40 mL). The reaction was stirred at room temperature for 3 h and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=85:15) yielded 175 mg (93%) of 4-cyclopropyl-2,6-dimethylphenol as a light yellow oil.

2-chloro-6-(4-cyclopropyl-2,6-dimethylphenoxy)-9H-purine

To a solution of 4-cyclopropyl-2,6-dimethylphenol (263 mg, 1.62 mmol) in 1-methyl-2-pyrridone (3 mL) at 0° C. was added NaH (65 mg, 1.62 mmol). The reaction mixture was stirred at room temperature for 30 min and a solution of 2,6-dichloropurine (102 mg, 0.54 mmol) in 1-methyl-2-pyrridone (2 mL) was added to the mixture. The mixture was heated at 100° C. for 16 h and then cooled to room temperature. The reaction was poured into ice water and extracted with CHCl₃ (3×20 mL). The combined organic solution was washed with H₂O (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (MeOH:CHCl₃=5:95) yielded 114 mg (67%) of 2-chloro-6-(4-cyclopropyl-2,6-dimethylphenoxy)-9H-purine.

4-(6-(4-cyclopropyl-2,6-dimethylphenoxy)-9H-purin-2-ylamino)benzonitrile

To a suspension of 2-chloro-6-(4-cyclopropyl-2,6-dimethylphenoxy)-91′-purine (28 mg, 0.088 mmol) and 4-aminobenzonitrile (42 mg, 0.35 mmol) in 2,2,2-trifluoroethanol (3 mL) in a sealed tube was added trifluoroacetic acid (0.056 mL, 0.70 mmol). The resulting solution was heated at 90° C. for 3 days. The reaction was cooled to room temperature and concentrated to dryness. Silica gel chromatography (CH₂Cl₂:Acetone=80:20) yielded 7 mg (20%) of 4-(6-(4-cyclopropyl-2,6-dimethylphenoxy)-9H-purin-2-ylamino)benzonitrile as a light yellow solid.

Example 7

2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidine

To a suspension of 4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (500 mg, 2.97 mmol) in 1,2-dichloroethane (40 mL) at −10° C. under argon was added antimony chloride (750 mg, 3.29 mmol). After stirring for 5 min, tert-butylnitrite (2.50 mL, 20.8 mmol) was added to the solution. The reaction was stirred at −10° C. for 3 h. The reaction was diluted with CHCl₃ (100 mL) and poured into ice water (50 mL). The CHCl₃ layer was separated, washed with brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=50:50) yielded 239 mg (43%) of 2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidine as a tan solid.

2-chloro-4-(4-cyclopropyl-2,6-dimethylphenoxy)-7H-pyrrolo[2,3-d]pyrimidine

To a solution of 4-cyclopropyl-2,6-dimethylphenol (259 mg, 1.60 mmol) in THF (3 mL) at 0° C. was added NaH (64 mg, 1.60 mmol). The reaction mixture was stirred at room temperature for 30 min and a solution of 2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidine (100 mg, 0.53 mmol) in THF (2 mL) was added to the mixture. The mixture was heated at 80° C. for 16 h and cooled to room temperature. The reaction was poured into ice water and extracted with CHCl₃ (3×20 mL). The combined organic solution was washed with H₂O (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 79 mg (48%) of 2-chloro-4-(4-cyclopropyl-2,6-dimethylphenoxy)-7H-pyrrolo[2,3-d]pyrimidine as a tan solid.

4-(4-(4-cyclopropyl-2,6-dimethylphenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)benzonitrile

To a suspension of 2-chloro-4-(4-cyclopropyl-2,6-dimethylphenoxy)-7H-pyrrolo[2,3-d]pyrimidine (75 mg, 0.24 mmol) and 4-aminobenzonitrile (113 mg, 0.96 mmol) in 2,2,2-trifluoroethanol (4 mL) in a sealed tube was added trifluoroacetic acid (0.15 mL, 1.92 mmol). The resulting solution was heated at 90° C. for 3 days. The reaction was diluted with EtOAc (50 mL), washed with NaHCO₃ (20 mL) and brine (20 mL), dried with Na₂SO₄, and concentrated to dryness. Silica gel chromatography (CH₂Cl₂:Acetone=90:10) yielded 15 mg (16%) of 4-(4-(4-cyclopropyl-2,6-dimethylphenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)benzonitrile as a tan solid.

Example 8

Scheme 1 illustrate the synthesis of 9-deazaguanine by starting with commercially available 2-amino-6-methylpyrimidin-4(3H)-one and nitrated with nitric acid followed by treatment of the nitrated product with N,N-dimethylformamide dimethyl acetal (DMF-DMA) to afford the corresponding 2-(dimethylamino)methyleneimino derivative. It was then benzylated to produce 3-benzyl-2-[(dimethylamino)methyleneimino]-5-nitro-6-methylpyrimidin-4-one by treating with benzyl bromide and converted to benzylated-2,6-bis-dimethylaminomethylene derivative with DMF-DMA. Reductive cyclization with sodium hydrosulfite followed by de-protection with 3M NaOH and de-benzylation with Pd/C and NH₄CO₂H afforded 9-deazaguanine.

Scheme 2 illustrates the 3 different pathways which provide the various substituted 9-deazapurines. Other products are synthesized by analogous methods, which a person skilled in the art could formulate, based on the reaction sequences given above. In certain cases, the person skilled in the art would see that protecting groups might be necessary. The synthetic scheme can be summarized as follows.

Benzylation of 9-deazaguanine followed by chlorination with POCl₃ gives the chlorinated 9-deazapurine product. This chlorinated intermediate can either be coupled with R2 (pathway 1) followed by diazotization with t-butyl nitrite; displaced with F; coupled with R3 and de-benzylated to give the product; or it can undergo pathway 2, which is diazotization with t-butyl nitrite in the presence of antimony chloride followed by coupling with R2 and R3, followed by de-benzylation to afford the final product. Alternatively, pathway 3 provides for de-benzylation of the dichloro-9-deazapurine followed by the coupling with R2 and R3 respectively to provide the various substituted 9-deazapurine.

2-Amino-6-methyl-5-nitropyrimidin-4(3H)-one

To a mixture of 2-amino-6-methylpyrimidin-4(3H)-one (50 g, 0.4 mol) in 250 mL of H₂SO₄ at 0° C. was added 40 mL of HNO₃ with an additional funnel. After being stirred at room temperature for 3 h, the reaction mixture was slowly poured into 3.6 L of diethyl ether and stirred for 15 min. Decant the ether solution and added 1.0 L of ethyl acetate to the solid and stirred for 10 h. The solid (54.8 g, 81% yield) was filtered and used for next step without any further purification.

(E)-N,N-Dimethyl-N′-(4-methyl-5-nitro-6-oxo-1,6-dihydropyrimidin-2-yl)formimidamide

To a suspension of 2-Amino-6-methyl-5-nitropyrimidin-4(3H)-one (54.8 g, 0.32 mol) in CH₂Cl₂ (461 mL) was added DMF-dimethylacetal (103.1 mL, 0.77 mol) and stirred at room temperature for 1.5 h. The reaction mixture was filtered, washed with CH₂Cl₂, and used for the next step without further purification (31.9 g, 44% yield).

(E)-N′(1-benzyl-4-methyl-5-nitro-6-oxo-1,6-dihydropyrimidin-2-yl)-N,N-dimethylformimidamide

To a suspension of (E)-N,N-Dimethyl-N′-(4-methyl-5-nitro-6-oxo-1,6-dihydropyrimidin-2-yl)formimidamide (53.4 g, 0.24 mmol) in DMF (690 mL) was added DBU (44.6 mL, 0.30 mol) and benzyl bromide (44.4 mL, 0.29 mol) and stirred at room temperature for 1 h. The excess of DBU was neutralized with HCl, and the mixture was concentrated in vacuo. The residue was dissolved in methylene chloride and extracted twice with 2M HCl and water, then dried over Na₂SO₄ and concentrated. Trituration with ethanol afforded the crystalline product which was washed with ethanol to give the product (64.7 g, 86% yield) and used in the next step without further purification.

(E)-N′-(1-benzyl-4-((E)-2-(dimethylamino)vinyl)-5-nitro-6-oxo-1,6-dihydropyrimidin-2-yl)-N,N-dimethylformimidamide

To a solution of (E)-N′(1-benzyl-4-methyl-5-nitro-6-oxo-1,6-dihydropyrimidin-2-yl)-N,N-dimethylformimidamide (64.7 g, 0.2 mol) in DMF (254 mL) was added DMF-dimethylacetal (54.5 mL, 0.41 mol). The reaction mixture was stirred for 3 h at 65° C., cooled, and the solvent was removed under reduced pressure. The residue was triturated with ethanol, and the solid was collected by vacuum filtration (69.2 g, 91%) and used in the next step without further purification.

(E)-N′-(3-benzyl-4-oxo-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-2-yl)-N,N-dimethylformimidamide

To a mixture of (E)-N′-(1-benzyl-4-((E)-2-(dimethylamino)vinyl)-5-nitro-6-oxo-1,6-dihydropyrimidin-2-yl)-N,N-dimethylformimidamide (43.0 g, 0.12 mol) in THF (151 mL) was added an aqueous saturated solution of Na₂S₂O₄ and stirred at room temperature overnight. Upon completion of the reaction, the solid was filtered and washed with THF to afford the product (21.2 g, 62% yield) which was used in the next step without further purification.

2-Amino-3-benzyl-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one

To a mixture of (E)-N′-(3-benzyl-4-oxo-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-2-yl)-N,N-dimethylformimidamide (21.2 g, 0.07 mol) in MeOH (382 mL) was added 3M NaOH (276 mL) and heated at 100° C. for 5 h. After completion of the reaction, the reaction mixture was cooled to 0° C. The solid was filtered (15.8 g, 91%) and used in the next step without further purification.

2-Amino-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one

To a mixture of 2-amino-3-benzyl-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one (10 g, 0.04 mol) in MeOH (334 mL) was added 10% Pd/C (2 g), ammonium formate (13.2 g, 0.21 mmol) and heated at 75° C. for 4 h. After completion of the reaction, the reaction mixture was cooled and filtered through a pad of Celite with hot 1:1 DMF/MeOH. The filtrate was concentrated in vacuo to provide the product as an off-white solid (6.2 g, 99%).

2-Amino-5-benzyl-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one

To a suspension of 2-amino-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one (336.7 mg, 2.0 mmol) in CH₂Cl₂ (14.3 mL) was added benzyl bromide (0.26 mL, 2.2 mmol) and TBABr (644 mg, 2.0 mmol). The reaction mixture was cooled to 0° C., and to it was added 50% NaOH (1.7 mL). The resulting mixture was stirred for 2 h as it warmed from 0° C. to room temperature. Water was then added, and the solution was washed with CHCl₃. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. Purification by column chromatography, eluting with CH₂Cl₂/Acetone (5:1-1:1), afforded the product as a tan solid (423 mg, 82%)

5-benzyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amine

A mixture of 2-amino-5-benzyl-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one (1.1 g, 7.4 mmol) and POCl₃ (7 mL, 74 mmol) was heated at 116° C. for 3 h. Upon completion of the reaction, the reaction mixture was poured into ice and extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. Purification by column chromatography, eluting with CH₂Cl₂/Acetone (3:1), afforded the product as a white solid (490 mg, 40%).

5-benzyl-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidin-2-amine

To a stirred suspension of NaH (56 mg, 2.33 mmol) in dry NMP (2 mL) was added 2,4,6-trimethyl phenol (317 mg, 2.33 mmol). The mixture was stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 5-benzyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amine (200 mg, 0.78 mmol) in dry NMP (1.5 mL) and the resulting solution was heated at 90° C. for 16 h. After completion of the reaction, the reaction mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with water, 2% NaOH, and brine and dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (3:1) to give the product as a white solid (140 mg, 50%).

5-benzyl-2-fluoro-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidine

A solution of 5-benzyl-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidin-2-amine (139.9 mg, 0.39 mmol) in pyridine (1.6 mL) was cooled to −50° C. and HF-pyr (8 mL) and t-butyl nitrite (0.19 mL, 1.56 mmol) was added dropwise. The reaction mixture was stirred at 50° C. to −30° C. for 1.5 h. Upon completion of the reaction, the reaction mixture was poured into K₂CO₃ (5 g), slowly added water and washed with CHCl₃×3. The combined organic layers were washed with brine, dried (Na₂SO₄), filtered and concentrated in vacuo. The crude product was purified by silica gel column chromatography, eluting with hexanes/ethyl acetate (2:1) to give the product as a white solid (116 mg, 82%).

4-(5-benzyl-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

A stirred suspension of NaH (63.8 mg, 2.66 mmol) in dry NMP (1.5 mL) was added 4-aminobenzylnitrile (188 mg, 2.66 mmol) and stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 5-benzyl-2-fluoro-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidine (115 mg, 0.32 mmol) in dry NMP (1.7 mL) and stirred at room temperature for 2 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc 3 times. The combined organic layers were washed with water, NH₄Cl, water×2, and brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with 1% MeOH:CH₂Cl₂, which afforded the product as a tan solid (120 mg, 80%).

4-(4-(Mesityloxy)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

To a suspension of 4-(5-benzyl-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile (150 mg, 0.33 mmol) in 1,2-dichlorobenzene (13 mL) was added AlCl₃ (436 mg, 3.27 mmol). The reaction mixture was heated at 160° C. for 1.5 h during which the reaction mixture became dark and homogeneous. Upon completion of the reaction, the reaction mixture was cooled and washed with NH₄Cl. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with Hexanes:Ethyl acetate (5:1-1:1) provided the product as a tan solid (27.8 mg, 23%).

Example 9

4-(2-Amino-5-benzyl-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

To a stirred suspension of NaH (155 mg, 6.47 mmol) in dry NMP (4 mL) was added 4-hydroxy-3,5-dimethylbenzonitrile (570 mg, 3.88 mmol), and the mixture was stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 5-benzyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amine (400 mg, 1.55 mmol) in dry NMP (4 mL) and heated at 160° C. for 16 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with water, 2% NaOH, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (2:1-1:4) to give the product as a light yellow solid (342 mg, 60%).

4-(5-benzyl-2-fluoro-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

A solution of 4-(2-amino-5-benzyl-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile (319.4 mg, 0.87 mmol) in pyridine (3 mL) was cooled to −50° C. and HF-pyr (15 mL) and t-butyl nitrite (0.42 mL, 3.46 mmol) were added dropwise. The reaction mixture was stirred at −50° C. to −20° C. for 1.5 h. Upon completion of the reaction, the mixture was poured into K₂CO₃ (8 g), diluted with water and washed with CHCl₃×3. The combined organic layers were washed with brine, dried (Na₂SO₄), filtered, and concentrated in vacuo. The crude product was purified by silica gel column chromatography, eluting with hexanes/ethyl acetate (2:1-1:1) which same the product as a light yellow solid (314 mg, 97%).

4-(5-benzyl-2-(4-cyanophenylamino)-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

To a stirred suspension of NaH (101 mg, 4.21 mmol) in dry NMP (4 mL) was added 4-aminobenzylnitrile (299 mg, 2.53 mmol) and stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 4-(5-benzyl-2-fluoro-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile (314 mg, 0.84 mmol) in dry NMP (4.4 mL) and stirred at room temperature for 2 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc×3. The combined organic layers were washed with water, NH₄Cl, water×2, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with 1% MeOH:CH₂Cl₂, producing the product as a tan solid (320 mg, 80%).

4-(2-(4-Cyanophenylamino)-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

To a suspension of 4-(5-benzyl-2-(4-cyanophenylamino)-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile (240 mg, 0.51 mmol) in 1,2-dichlorobenzene (20 mL) was added AlCl₃ (681 mg, 5.1 mmol). The reaction mixture was heated at 160° C. for 1.5 h, during which time the reaction mixture became dark and homogeneous. Upon completion of the reaction, the reaction mixture was cooled and washed with NH₄Cl. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered and concentrated in vacuo. The crude product was purified by preparative TLC TLC eluting with Hexanes:Ethyl acetate (2.5:1) and produced the product as a pink solid (51 mg, 26%).

Example 10

5-benzyl-4-(mesitylthio)-5H-pyrrolo[3,2-d]pyrimidin-2-amine

To a stirred suspension of NaH (48 mg, 2 mmol) in dry NMP (2 mL) was added 2,4,6-trimethyl-benzene-1-thiol (191 mg, 1.2 mmol) The mixture was and stirred at room temperature for 30 min under argon. The reaction mixture was then added to a solution of 5-benzyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amine (103 mg, 0.4 mmol) in dry NMP (2.5 mL) and heated at 60° C. for 16 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with water, 2% NaOH, and brine; dried over Na₂SO₄; filtered; and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (2:1-1:3) to give the product as a light yellow solid (131 mg, 88%).

5-benzyl-2-fluoro-4-(mesitylthio)-5H-pyrrolo[3,2-d]pyrimidine

A solution of 5-benzyl-4-(mesitylthio)-5H-pyrrolo[3,2-d]pyrimidin-2-amine (131 mg, 0.35 mmol) in pyridine (1.6 mL) was cooled to −50° C. and added HF-pyr (8 mL) and t-butyl nitrite (0.17 mL, 1.4 mmol) dropwise. The reaction mixture was stirred at −50° C. to −40° C. for 1.5 h. Upon completion of the reaction, the reaction was poured into K₂CO₃ (5 g), slowly added water and washed with CHCl₃×3. The combined organic layers were washed with brine, dried (Na₂SO₄), filtered and concentrated in vacuo. The crude product was purified by silica gel column chromatography, eluting with hexanes/ethyl acetate (5:1-1:1) to give the product as an off-white solid (94 mg, 71%).

4-(5-benzyl-4-(mesitylthio)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

To a stirred suspension of NaH (30 mg, 1.25 mmol) in dry NMP (1.5 mL) was added 4-aminobenzylnitrile (87.4 mg, 0.74 mmol) and stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 5-benzyl-2-fluoro-4-(mesitylthio)-5H-pyrrolo[3,2-d]pyrimidine (93 mg, 0.25 mmol) in dry NMP (1 mL) and stirred at room temperature for 2 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc×3. The combined organic layers were washed with water, NH₄Cl, water×2, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by preparative TLC TLC, eluting with Hexanes:Ethyl acetate (1.5:1) afforded the product as a tan solid (12.6 mg, 11%).

4-(4-(mesitylthio)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

To a suspension of 4-(5-benzyl-4-(mesitylthio)-5H-pyrrolo[3,2-a]pyrimidin-2-ylamino)benzonitrile (9.2 mg, 0.03 mmol) in 1,2-dichlorobenzene (1 mL) was added AlCl₃ (26 mg, 0.3 mmol). The reaction mixture was heated at 160° C. for 1.5 h, which the reaction mixture became dark and homogeneous. Upon completion of the reaction, the reaction mixture was cooled and washed with NH₄Cl. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by preparative TLC TLC, eluting with Hexanes:Ethyl acetate (2.5:1) produced the product as a pink solid (7.7 mg, 20%).

Example 11

5-benzyl-2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidine

To a suspension of 5-benzyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amine (641 mg, 2.5 mmol) in 1,2-dichloroethane (35 mL) was cooled to −10° C. SbCl₃ (850 mg, 3.7 mmol) was added. The reaction mixture was stirred for 5 min. t-butyl nitrite (2.1 mL, 17.4 mmol) was added dropwise and the stirred mixture was from −10° C. to room temperature for 5 h. Upon completion of the reaction, the reaction mixture was poured into ice water and washed with CH₂Cl₂. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered and concentrated in vacuo. The crude product was purified by silica gel column chromatography eluting with Hexanes:Ethyl acetate (9:1-1:1), and gave the product as an off-white solid (528 mg, 77%).

2,4-Dichloro-5H-pyrrolo[3,2-d]pyrimidine

To a suspension of 5-benzyl-2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidine (177 mg, 0.64 mmol) in 1,2-dichlorobenzene (20 mL) was added AlCl₃ (852 mg, 6.4 mmol). The reaction mixture was heated at 160° C. for 1.5 h, during which the reaction mixture became dark and homogeneous. Upon completion of the reaction, the reaction mixture was cooled, added CHCl₃ and washed with NH₄Cl. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. Added Hexanes and filtered off the product as purple solids (100 mg, 80%) and used for the next step without further purification.

2-Chloro-4-(4-cyclopropyl-2,6-dimethylphenoxy)-5H-pyrrolo[3,2-d]pyrimidine

To a stirred suspension of NaH (25 mg, 0.64 mmol) in dry NMP (1.5 mL) was added 4-cyclopropyl-2,6-dimethylphenol (103 mg, 0.64 mmol) and the resolution mixture was stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidine (120 mg, 0.64 mmol) in dry NMP (1.7 mL) and heated at 90° C. for 16 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with water, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (4:1-2:1), to give the product as a light yellow solid (20.2 mg, 8%).

4-(4-(4-Cyclopropyl-2,6-dimethylphenoxy)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

In a sealed tube was placed 2-chloro-4-(4-cyclopropyl-2,6-dimethylphenoxy)-5H-pyrrolo[3,2-d]pyrimidine (20 mg, 0.064 mmol), 4-aminobenzonitrile (31 mg, 0.26 mmol), TFE (0.21 mL) and TFA (0.04 mL, 0.51 mmol). The reaction mixture was stirred at 90° C. for 16 h. Upon completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with NaHCO₃, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by preparative TLC TLC, eluting with 5% Acetone/CH₂Cl₂ to give the product as a light yellow solid (10.5 mg, 45%).

Example 12

2-Chloro-4-(mesityloxy)-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

To a stirred suspension of NaH (8.9 mg, 0.22 mmol) in dry NMP (1.0 mL) was added 2,4,6-trimethyl phenol (30.2 mg, 0.22 mmol) and stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 2,4-dichloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine (44.6 mg, 0.22 mmol) in dry NMP (1.0 mL) and heated at 90° C. for 16 h. After completion of the reaction, the resulting mixture was cooled, diluted with water and washed with EtOAc. The combined organic layers were washed with water, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (5:1-2:1), to give the product as a light yellow solid (52.7 mg, 80%).

4-(4-(Mesityloxy)-5-methyl-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

In a sealed tube was added 2-chloro-4-(mesityloxy)-5-methyl-5H-pyrrolo[3,2-d]pyrimidine (52.7 mg, 0.18 mmol), 4-aminobenzonitrile (83 mg, 0.70 mmol), TFE (1.0 mL) and TFA (0.11 mL, 1.44 mmol). The reaction mixture was stirred at 90° C. for 48 h. Upon completion of the reaction, the resulting mixture was cooled, diluted with water and washed with EtOAc. The combined organic layers were washed with NaHCO₃, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by preparative TLC, eluting with hexanes:ethyl acetate (5:1-2:1), to give the product as a light yellow solid

4-(2-Chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

To a stirred solution of NaH (42.1 mg, 1.05 mmol) in dry NMP (2.5 mL) was added 4-hydroxy-3,5-dimethylbenzonitrile (154.7 mg, 1.05 mmol) and stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 2,4-dichloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine (211.3 mg, 1.05 mmol) in dry NMP (2.7 mL) and heated at 160° C. for 16 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with water, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (3:1-1:1), to give the product as a light yellow solid (294 mg, 85%).

4-(2-(4-Cyanophenylamino)-5-methyl-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

In a sealed tube was added 4-(2-chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile (294 mg, 0.94 mmol), 4-aminobenzonitrile (455 mg, 3.77 mmol), TFE (3.1 mL) and TFA (0.58 mL, 7.52 mmol). The reaction mixture was stirred at 90° C. for 48 h. Upon completion of the reaction, the resulting mixture was cooled, diluted with water and washed with EtOAc. The combined organic layers were washed with NaHCO₃, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by preparative TLC, eluting with hexanes:ethyl acetate (4:1-1:2), to give the product as an off-white solid (133 mg, 40%).

Example 13

1-(4-(5-benzyl-2-chloro-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylphenyl)ethanone

To a stirred solution of NaH (31 mg, 0.78 mmol) in dry NMP (2 mL) was added 1-(4-hydroxy-3,5-dimethylphenyl)ethanone (127 mg, 0.78 mmol) and stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 5-benzyl-2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidine (216 mg, 0.78 mmol) in dry NMP (2.4 mL) and heated at 160° C. for 16 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with water, 2% NaOH, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (4:1-2:1), to give the product as a light yellow solid (111 mg, 35%).

4-(4-(4-Acetyl-2,6-dimethylphenoxy)-5-benzyl-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

In a sealed tube was added 1-(4-(5-benzyl-2-chloro-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylphenyl)ethanone (111 mg, 0.27 mmol), 4-aminobenzonitrile (129 mg, 1.1 mmol), TFE (1.7 mL) and TFA (0.2 mL, 2.16 mmol). The reaction mixture was stirred at 90° C. for 16 h. Upon completion of the reaction, the resulting mixture was cooled, diluted with water, and washed with EtOAc. The combined organic layers were washed with NaHCO₃ and brine; dried over Na₂SO₄; filtered; and concentrated in vacuo. The crude product was purified by silica gel column chromatography, eluting with hexanes:ethyl acetate (9:1-100% EtOAc), to give the product as an off-white solid (68 mg, 51%).

4-(4-(4-Acetyl-2,6-dimethylphenoxy)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

To a suspension of 4-(4-(4-acetyl-2,6-dimethylphenoxy)-5-benzyl-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile (65 mg, 0.13 mmol) in 1,2-dichlorobenzene (5.3 mL) was added AlCl₃ (178 mg, 1.3 mmol). The reaction mixture was heated at 160° C. for 1.5 h, after which time the reaction mixture became dark and homogeneous. Upon completion of the reaction, the reaction mixture was cooled, CHCl₃ was added, and the mixture was washed with NH₄Cl. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by silica gel column chromatography, eluting with hexanes:ethyl acetate (3:1), to give the product as a brown solid (41 mg, 77%).

Example 14

1-(4-(5-benzyl-2-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylphenyl)-N,N-dimethylmethanamine

To a stirred solution of NaH (80.4 mg, 1.0 mmol) in dry NMP (3 mL) was added 4-((dimethylamino)methyl)-2,6-dimethylphenol (216.4 mg, 1.0 mmol) and the mixture was stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 5-benzyl-2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidine (216 mg, 0.78 mmol) in dry NMP (2.6 mL) and heated at 120° C. for 16 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc. The combined organic layers were washed twice with water, washed with, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by silica gel column chromatography, eluting with MeOH/CH₂Cl₂ (10%-30%), to give the product as a tan solid (71 mg, 17%).

4-(5-benzyl-4-(4-((dimethylamino)methyl)-2,6-dimethylphenoxy)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

In a sealed tube was added 1-(4-(5-benzyl-2-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylphenyl)-N,N-dimethylmethanamine (70.7 mg, 0.17 mmol), 4-aminobenzonitrile (78.9 mg, 0.67 mmol), TFE (1.1 mL) and TFA (0.1 mL, 1.3 mmol). The reaction mixture was stirred at 90° C. for 16 h. Upon completion of the reaction, the resulting mixture was cooled, diluted with water, and washed with EtOAc. The combined organic layers were washed with NaHCO₃ solution and with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by silica gel column chromatography, eluting with MeOH/CH₂Cl₂ (20%-40%), to give the product as a tan solid (17 mg, 20%).

4-(4-(4-((dimethylamino)methyl)-2,6-dimethylphenoxy)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

The benzyl group was removed according to the same procedure as described for example 13.

Example 15

5-benzyl-2-chloro-4-(2,6-dimethyl-4-nitrophenoxy)-5H-pyrrolo[3,2-d]pyrimidine

To a stirred solution of NaH (61.9 mg, 2.6 mmol) in dry NMP (4.7 mL) was added 2,6-dimethyl-4-nitrophenol (258.9 mg, 1.55 mmol) and stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 5-benzyl-2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidine (431 mg, 1.55 mmol) in dry NMP (4 mL) and heated at 90° C. for 16 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc. The combined organic layers were washed twice with water, washed with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by silica gel column chromatography, eluting with hexanes:ethyl acetate (3:1-1:1), to give the product as a white solid (598 mg, 94%).

4-(5-benzyl-4-(2,6-dimethyl-4-nitrophenoxy)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

In a sealed tube was added 5-benzyl-2-chloro-4-(2,6-dimethyl-4-nitrophenoxy)-5H-pyrrolo[3,2-d]pyrimidine (598 mg, 1.46 mmol), 4-aminobenzonitrile (691 mg, 5.85 mmol), TFE (9.1 mL) and TFA (1.97 mL, 11.7 mmol). The reaction mixture was stirred at 90° C. for 16 h. Upon completion of the reaction, the resulting mixture was cooled, diluted with water and washed with EtOAc. The combined organic layers were washed with NaHCO₃, brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by silica gel column chromatography, eluting with hexanes:ethyl acetate (3:1-1:1), to give the product (442 mg, 60%).

Example 16

4-(4-(4-Acetyl-2,6-dimethylphenoxy)-7-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

To a solution of 4-(4-(4-acetyl-2,6-dimethylphenoxy)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile (13 mg, 0.03 mmol) in CH₂Cl₂ (1 mL) was added NCS (4.4 mg, 0.03 mmol) and the mixture refluxed for 16 h. After the completion of the reaction, the solvent was concentrated and purified by preparative TLC eluting with hexanes:ethyl acetate (2:1) to give the product (4.2 mg, 30%).

Example 17

4-(7-Chloro-4-(mesitylthio)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

To a solution of 4-(4-(mesitylthio)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile (10 mg, 0.02 mmol) in CH₂Cl₂ (5 mL) was added NCS (2.8 mg, 0.02 mmol) and the resolution mixture refluxed for 16 h. After the completion of the reaction, the solvent was concentrated and purified by preparative TLC, eluting with hexanes:ethyl acetate (3:1), to give the product (8.8 mg, 88%).

Example 18

4-(7-bromo-4-(mesitylthio)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

To a solution of 4-(4-(mesitylthio)-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile (22.7 mg, 0.06 mmol) in CH₂Cl₂ (10 mL) was added NBS (10.5 mg, 0.06 mmol) and the resultant mixture was refluxed for 16 h. After completion of the reaction, the solvent was concentrated and purified by reversed phase HPLC to give the product as a white solid (6.4 mg, 23%).

Example 19

4-(7-chloro-4-(mesityloxy)-5-methyl-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

To a solution of 4-(4-(mesityloxy)-5-methyl-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile (17.3 mg, 0.05 mmol) in CH₂Cl₂ (5 mL) was added NCS (6.03 mg, 0.05 mmol) and the resultant mixture was refluxed for 16 h. After completion of the reaction, the solvent was concentrated and purified by preparative TLC, eluting with hexanes:ethyl acetate (3:1), to give the product as an off-white solid (3.4 mg, 6%).

Example 20

4-(7-Chloro-2-(4-cyanophenylamino)-5-methyl-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

To a solution of 4-(2-(4-cyanophenylamino)-5-methyl-5H-pyrrolo[3,2-a]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile (21.5 mg, 0.06 mmol) in CH₂Cl₂ (3 mL) was added NCS (7.3 mg, 0.06 mmol) and the resultant mixture was refluxed for 16 h. After completion of the reaction, the solvent was concentrated and purified by preparative TLC, eluting with Hexanes:Ethyl acetate (3:1), to give the product as a light yellow solid (13.2 mg, 56%).

Example 21

4-(7-Bromo-2-(4-cyanophenylamino)-5-methyl-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

To a solution of 4-(2-(4-cyanophenylamino)-5-methyl-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile (58 mg, 0.15 mmol) in CH₂Cl₂ (8 mL) was added NBS (29 mg, 0.16 mmol) and the resultant mixture was refluxed for 16 h. After completion of the reaction, the solvent was concentrated and purified by preparative TLC, eluting with hexanes:ethyl acetate (2:1), to give the product as a yellow solid (40 mg, 57%).

Example 22

4-(7-Chloro-2-(4-cyanophenylamino)-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

To a solution of 4-(2-(4-cyanophenylamino)-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile (28.1 mg, 0.07 mmol) in CH₂Cl₂ (4 mL) was added NCS (9.9 mg, 0.07 mmol) and the resultant mixture was refluxed for 16 h. After completion of the reaction, the solvent was concentrated and purified by preparative TLC eluting with hexanes:ethyl acetate (2:1), to give the product as a pink solid (20 mg, 65%).

Biological Activity

Inhibition of HIV-1 Reverse Transcriptase

Numerous compounds were screened for inhibitory activity against human immunodeficiency virus type 1 (HIV-1) using a high throughput cell-based assay using HIV-1 expressing firefly luciferase as a reporter gene and pseudotyped with vesicular stomatitis virus envelope glycoprotein (VSV-G). Experimental procedures were essentially as described by Connor et al. in Journal of Virology (1996), 70: 5306-5311 (Characterization of the functional properties of env genes from long-term survivors of human immunodeficiency virus type 1 infection), and Popik et al. in Journal of Virology (2002), 76: 4709-4722 (Human immunodeficiency virus type 1 uses lipid raft-co-localized CD4 and chemokine receptors for productive entry into CD4+ T cells). It should be particularly appreciated that the virus contains two introduced mutations in the RT gene (K103N and Y181C, created by PCR mutagenesis) that render the virus highly resistant to current non-nucleoside HIV-1 drugs. Virus stocks were generated by cotransfection of plasmid DNA encoding VSV-G with vector pNL4-3Env(−)Luc(+) into 293T cells. Sixty-four hours after transfection, virus-containing medium was collected by centrifugation and stored frozen at −80° C.

HeLa cells were infected with the VSV-G pseudotyped virus in the presence of screening compounds in a 384-well microtiter plate format. Forty-eight hours after initial infection, lysis buffer and Luciferase Assay Reagent (Promega) was added to the cells and luciferase activity was determined by counting the resultant luminescence using a LJL luminometer. Since the luciferase gene is carried in the virus genome, its expression level directly reflects the virus replication level in the presence of a compound.

To evaluate the activity of the compounds against wild type HIV-1, the HeLa-JC53 cell line that expresses high levels of CD4 and CCR5 (see e.g., Platt et al. in Journal of Virology (1998), 72: 2855-2864: Effect of CCR5 and CD4 cell surface concentrations on infection by macrophagetropic isolates of human immunodeficiency virus type 1) was modified by isolation of a stable cell line that expresses luciferase under the control of the HIV-1 promoter (long terminal repeat, i.e., LTR). HIV-1 infection of this cell line stimulates the transcription of luciferase from the HIV-1 promoter and the luciferase gene expression level is proportional to the level of virus replication (Harrington et al. in Journal of Virology Methods (2000), 88: 111-115: Direct detection of infection of HIV-1 in blood using a centrifugation-indicator cell assay; and Roos et al. in Virology (2000), 273: 307-315: LuSIV cells: a reporter cell line for the detection and quantitation of a single cycle of HIV and SW replication). Procedures for virus infection, compound testing and luciferase activity determination were the same as for the VSV-G pseudotyped HIV-1.

Two approaches were used to evaluate the cytotoxicity of the positive compounds discovered in the HIV-1 virus assays. The first approach employed another modified HeLa-JC53 cell line that constitutively expresses high level of luciferase without virus infection. The level of luciferase expression in these cells served as an indicator for cell replication in the presence of the compounds. Procedures for compound testing and luciferase activity determination were the same as for the virus infection tests. The other toxicity assay utilized HeLe-JC53 cells and a commercially available MTS assay kit (Promega) that measures the mitochondria function of the cells.

Results

The results are listed in Table A as EC50 (nM) and IC50 (nM). Table legend: A is <10, B is between 10 and 100, C is >100, ND is not determined. Note that many compounds of this invention exhibit activities on wild-type (WT) and resistant mutants below 10 nM.

TABLE A EC₅₀ EC₅₀ WT EC₅₀ EC₅₀ L100I- Cpd Structure (nM) Y181C (nM) Y188L (nM) K103N (nM) 1

A B B B CLogP: 6.31119 2

A B B C CLogP: 7.1942 3

A A A A CLogP: 5.24519 4

A B B B CLogP: 7.00339 5

A A A A CLogP: 5.71888 6

A B B B CLogP: 6.67519 7

A A B B CLogP: 5.85982 8

B C C C CLogP: 8.36608 9

A C C C CLogP: 5.81219 10

A B B B CLogP: 6.65919 11

A B A B CLogP: 6.5252 12

B C C C CLogP: 4.43498 13

A A A A CLogP: 5.18408 14

A C C C CLogP: 6.24839 15

B C C C CLogP: 4.67978 16

C C C C CLogP: 6.01359 17

A B A B CLogP: 4.79382 18

B C C C CLogP: 7.04473 19

A A A B CLogP: 6.16288 20

A B C C CLogP: 6.67638 21

A B B C CLogP: 6.10888 22

A C C C CLogP: 7.12038 23

A A A B CLogP: 6.50038 24

B C C C CLogP: 4.46648 25

A A A B CLogP: 4.65288 26

A B B C CLogP: 5.71308 27

A B B B CLogP: 7.17134 28

A A B B CLogP: 6.94438 29

A C C C CLogP: 6.01638 30

C C C C CLogP: 5.42063 31

A B A B CLogP: 6.34288 32

A B C C CLogP: 6.67638 33

A B B B CLogP: 6.75519 34

A A B B CLogP: 6.41174 35

A B C C CLogP: 6.18265 36

A B C C CLogP: 5.71888 37

A A A A CLogP;: 6.52119 38

B C C C CLogP: 7.16147 39

C C C C CLogP: 7.16147 40

B B C B CLogP: 6.60982 41

A A B B CLogP: 7.16208 42

A A A A CLogP: 5.45519 43

B B C B CLogP: 6.95418 44

B C C C CLogP: 7.19878 45

A A A B CLogP: 5.46143 46

C C C C CLogP: 6.29507 47

B B C C CLogP: 8.67208 48

B B C C CLogP: 9.11123 49

A A A A CLogP: 6.18873 50

A A B C CLogP: 4.02888 51

A A A B CLogP: 7.4042 52

A A A A CLogP: 6.96519 53

A B B C CLogP: 8.13777 54

A B B C CLogP: 9.83084 55

A B B C CLogP: 8.28777 56

B B B B CLogP: 7.88168 57

A A A A CLogP: 6.46008 58

B B C C CLogP: 8.59208 59

B B B B CLogP: 7.17968 60

A A B B CLogP: 7.16808 61

A A A A CLogP: 5.46119 62

A A A A CLogP: 7.39368 63

B B C C CLogP: 8.44208 64

A B C C CLogP: 8.22808 65

A A A C CLogP: 6.02219 66

A A A A CLogP: 6.73519 67

A A B A CLogP: 6.19473 68

A A A A CLogP: 5.39408 69

A A A A CLogP: 6.11368 70

A A A A CLogP: 6.26368 71

A A A A CLogP: 6.86919 Contemplated Compounds and Prophetic Examples

In addition to the examples listed above, this invention provides or contemplates many compounds, examples of which are shown in the tables that follow.

TABLE 1 Contemplated Compounds of Formula IA-1 IA-1

Ar V W Z  1. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN H CH₃  2. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN benzyl CH₃  3. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN benzyl H  4. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN 3-Me-benzyl CH₃  5. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN 4-Me-benzyl H  6. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN 3-MeO-benzyl H  7. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN 4-MeO-benzyl CH₃  8. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN H H  9. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN H Br  10. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN cyclopropyl CH₂CH₃  11. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN CH₂CF₃ CH₂CH₃  12. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN H CH₃  13. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN benzyl CH₃  14. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN benzyl H  15. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN 3-Me-benzyl cyclopropyl  16. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN 3-MeO-benzyl benzyl  17. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN H H  18. o,o′-diCH₃O-p-(CH═CHCN)phenyl C≡CCH₃ CH₂CH₃ CH₃  19. o,o′-diCH₃O-p-(CH═CHCN)phenyl Cl CH₂CH═CH₂ H  20. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂CH₃ CH₂CH═CH₂ H  21. o,o′-diCH₃O-p-(CH═CHCN)phenyl Cl CH₂CH₃ CH₂CH₃  22. o,o′-diCH₃O-p-(CH═CHCN)phenyl Cl H H  23. 4-cyclopropylnaphth-1-yl CN H CH₃  24. 4-cyclopropylnaphth-1-yl CN benzyl CH₃  25. 4-cyclopropylnaphth-1-yl CN benzyl H  26. 4-cyclopropylnaphth-1-yl CN H H  27. 4-cyclopropylnaphth-1-yl CH═CHCN H CH₃  28. 4-cyclopropylnaphth-1-yl CH═CHCN benzyl CH₃  29. 4-cyclopropylnaphth-1-yl CH═CHCN benzyl H  30. 4-cyclopropylnaphth-1-yl CH═CHCN H H  31. 4-cyclopropylnaphth-1-yl SO₂NHCH₃ CH₂CN F  32. 4-cyclopropylnaphth-1-yl SO₂NHCH₃ cyclopropyl Cl  33. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₂CH₂CN Br  34. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₂CN benzyl  35. o,o′-di-CH₃O-p-CN-phenyl C≡CCH₃ 3-MeO-benzyl F  36. o,o′-di-CH₃O-p-CN-phenyl F 3-Me-benzyl Cl  37. o,o′-di-CH₃O-p-CN-phenyl CN H CH₃  38. o,o′-di-CH₃O-p-CN-phenyl CN benzyl CH₃  39. o,o′-di-CH₃O-p-CN-phenyl CN benzyl H  40. o,o′-di-CH₃O-p-CN-phenyl CN H H  41. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H CH₃  42. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN benzyl CH₃  43. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN benzyl H  44. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H H  45. o,o′-di-CH₃-p-CN-phenyl CN H CH₃  46. o,o′-di-CH₃-p-CN-phenyl CN benzyl CH₃  47. o,o′-di-CH₃-p-CN-phenyl CN 3,5-di MeO-benzyl CH₃  48. o,o′-di-CH₃-p-CN-phenyl CN benzyl H  49. o,o′-di-CH₃-p-CN-phenyl CN H H  50. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H CH₃  51. o,o′-di-CH₃-p-CN-phenyl CH═CHCN benzyl CH₃  52. o,o′-di-CH₃-p-CN-phenyl CH═CHCN benzyl H  53. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H H  54. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN H F  55. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN benzyl F  56. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN benzyl F  57. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN H F  58. 4-cyclopropylnaphth-1-yl CN H F  59. 4-cyclopropylnaphth-1-yl CN benzyl F  60. 4-cyclopropylnaphth-1-yl CH═CHCN H F  61. 4-cyclopropylnaphth-1-yl CH═CHCN benzyl F  62. o,o′-di-CH₃O-p-CN-phenyl CN H F  63. o,o′-di-CH₃O-p-CN-phenyl CN benzyl F  64. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H F  65. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN benzyl F  66. o,o′-di-CH₃-p-CN-phenyl CN H F  67. o,o′-di-CH₃-p-CN-phenyl CN benzyl F  68. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H F  69. o,o′-di-CH₃-p-CN-phenyl CH═CHCN benzyl F  70. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ H CH₃  71. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ benzyl CH₃  72. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ benzyl H  73. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ H H  74. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ H CH₃  75. o,o′-diCH₃O-p-(CH═CHCN)phenyl F benzyl CH₃  76. o,o′-diCH₃O-p-(CH═CHCN)phenyl F benzyl H  77. o,o′-diCH₃O-p-(CH═CHCN)phenyl F H H  78. 4-cyclopropylnaphth-1-yl SO₂NH₂ H CH₃  79. 4-cyclopropylnaphth-1-yl SO₂NH₂ benzyl CH₃  80. 4-cyclopropylnaphth-1-yl SO₂NH₂ benzyl H  81. 4-cyclopropylnaphth-1-yl SO₂NH₂ H H  82. 4-cyclopropylnaphth-1-yl F H CH₃  83. 4-cyclopropylnaphth-1-yl F benzyl CH₃  84. 4-cyclopropylnaphth-1-yl F benzyl H  85. 4-cyclopropylnaphth-1-yl F H H  86. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H CH₃  87. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ benzyl CH₃  88. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ benzyl H  89. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H H  90. o,o′-di-CH₃O-p-CN-phenyl F H CH₃  91. o,o′-di-CH₃O-p-CN-phenyl F benzyl CH₃  92. o,o′-di-CH₃O-p-CN-phenyl F benzyl H  93. o,o′-di-CH₃O-p-CN-phenyl F H H  94. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H CH₃  95. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ benzyl CH₃  96. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ 3-Me-benzyl CH₃  97. o,o′-di-CH₃-p-CN-phenyl SO₂NHCH₃ benzyl H  98. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ benzyl H  99. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H H 100. o,o′-di-CH₃-p-CN-phenyl F H CH₃ 101. o,o′-di-CH₃-p-CN-phenyl F benzyl CH₃ 102. o,o′-di-CH₃-p-CN-phenyl F benzyl H 103. o,o′-di-CH₃-p-CN-phenyl F H H 104. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ H F 105. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ benzyl F 106. o,o′-diCH₃O-p-(CH═CHCN)phenyl F benzyl F 107. o,o′-diCH₃O-p-(CH═CHCN)phenyl F H F 108. 4-cyclopropylnaphth-1-yl SO₂NH₂ H F 109. 4-cyclopropylnaphth-1-yl SO₂NH₂ benzyl F 110. 4-cyclopropylnaphth-1-yl F H F 111. 4-cyclopropylnaphth-1-yl F benzyl F 112. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H F 113. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ benzyl F 114. o,o′-di-CH₃O-p-CN-phenyl F H F 115. o,o′-di-CH₃O-p-CN-phenyl F benzyl F 116. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H F 117. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ benzyl F 118. o,o′-di-CH₃-p-CN-phenyl F H F 119. o,o′-di-CH₃-p-CN-phenyl F benzyl F 120. 2,4,6-trimethyl phenyl CN H CH₃ 121. 2,4,6-trimethyl phenyl CN benzyl CH₃ 122. 2,4,6-trimethyl phenyl CN benzyl H 123. 2,4,6-trimethyl phenyl CN H H 124. 2,4,6-trimethyl phenyl CH═CHCN H CH₃ 125. 2,4,6-trimethyl phenyl CH═CHCN benzyl CH₃ 126. 2,4,6-trimethyl phenyl CH═CHCN benzyl H 127. 2,4,6-trimethyl phenyl CH═CHCN H H 128. 2,4,6-trimethyl phenyl CN H F 129. 2,4,6-trimethyl phenyl CN benzyl F 130. 2,4,6-trimethyl phenyl CH═CHCN H F 131. 2,4,6-trimethyl phenyl CH═CHCN benzyl F 132. 2,4,6-trimethyl phenyl SO₂NH₂ H CH₃ 133. 2,4,6-trimethyl phenyl SO₂NH₂ benzyl CH₃ 134. 2,4,6-trimethyl phenyl SO₂NH₂ benzyl H 135. 2,4,6-trimethyl phenyl SO₂NH₂ H H 136. 2,4,6-trimethyl phenyl F H CH₃ 137. 2,4,6-trimethyl phenyl F benzyl CH₃ 138. 2,4,6-trimethyl phenyl F benzyl H 139. 4-cyclopropyl phenyl F H H 140. 4-cyclopropyl phenyl SO₂NH₂ H F 141. 4-cyclopropyl phenyl SO₂NH₂ benzyl F 142. 4-cyclopropyl phenyl F H F 143. 4-cyclopropyl phenyl F benzyl F 144. o,o′-dimethyl-p-cyclopropyl phenyl CN H CH₃ 145. o,o′-dimethyl-p-cyclopropyl phenyl CN benzyl CH₃ 146. o,o′-dimethyl-p-cyclopropyl phenyl CN benzyl H 147. o,o′-dimethyl-p-cyclopropyl phenyl CN H H 148. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H CH₃ 149. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN benzyl CH₃ 150. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN benzyl H 151. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H H 152. o,o′-dimethyl-p-cyclopropyl phenyl CN H F 153. o,o′-dimethyl-p-cyclopropyl phenyl CN benzyl F 154. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H F 155. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN benzyl F 156. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H CH₃ 157. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ benzyl CH₃ 158. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ benzyl H 159. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H H 160. o,o′-dimethyl-p-cyclopropyl phenyl F H CH₃ 161. o,o′-dimethyl-p-cyclopropyl phenyl F benzyl CH₃ 162. o,o′-dimethyl-p-cyclopropyl phenyl F benzyl H 163. o,o′-dimethyl-p-cyclopropyl phenyl F H H 164. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H F 165. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ benzyl F 166. o,o′-dimethyl-p-cyclopropyl phenyl F H F 167. o,o′-dimethyl-p-cyclopropyl phenyl F benzyl F 168. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN CH₃ CH₃ 169. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN cyclopropyl CH₃ 170. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN cyclopropyl H 171. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN CH₃ H 172. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN CH₃ CH₃ 173. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN cyclopropyl CH₃ 174. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN cyclopropyl H 175. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN CH₃ H 176. 4-cyclopropylnaphth-1-yl CN CH₃ CH₃ 177. 4-cyclopropylnaphth-1-yl CN cyclopropyl CH₃ 178. 4-cyclopropylnaphth-1-yl CN cyclopropyl H 179. 4-cyclopropylnaphth-1-yl CN CH₃ H 180. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ CH₃ 181. 4-cyclopropylnaphth-1-yl CH═CHCN cyclopropyl CH₃ 182. 4-cyclopropylnaphth-1-yl CH═CHCN cyclopropyl H 183. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ H 184. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ CH₃ 185. o,o′-di-CH₃O-p-CN-phenyl CN cyclopropyl CH₃ 186. o,o′-di-CH₃O-p-CN-phenyl CN cyclopropyl H 187. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ H 188. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ CH₃ 189. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN cyclopropyl CH₃ 190. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN cyclopropyl H 191. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ H 192. o,o′-di-CH₃-p-CN-phenyl CN CH₃ CH₃ 193. o,o′-di-CH₃-p-CN-phenyl CN cyclopropyl CH₃ 194. o,o′-di-CH₃-p-CN-phenyl CN cyclopropyl H 195. o,o′-di-CH₃-p-CN-phenyl CN CH₃ H 196. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ CH₃ 197. o,o′-di-CH₃-p-CN-phenyl CH═CHCN cyclopropyl CH₃ 198. o,o′-di-CH₃-p-CN-phenyl CH═CHCN cyclopropyl H 199. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ H 200. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN CH₃ F 201. o,o′-diCH₃O-p-(CH═CHCN)phenyl CN cyclopropyl F 202. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN cyclopropyl F 203. o,o′-diCH₃O-p-(CH═CHCN)phenyl CH═CHCN CH₃ F 204. 4-cyclopropylnaphth-1-yl CN CH₃ F 205. 4-cyclopropylnaphth-1-yl CN cyclopropyl F 206. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ F 207. 4-cyclopropylnaphth-1-yl CH═CHCN cyclopropyl F 208. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ F 209. o,o′-di-CH₃O-p-CN-phenyl CN cyclopropyl F 210. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ F 211. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN cyclopropyl F 212. o,o′-di-CH₃-p-CN-phenyl CN CH₃ F 213. o,o′-di-CH₃-p-CN-phenyl CN cyclopropyl F 214. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ F 215. o,o′-di-CH₃-p-CN-phenyl CH═CHCN cyclopropyl F 216. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ CH₃ CH₃ 217. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ cyclopropyl CH₃ 218. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ cyclopropyl H 219. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ CH₃ H 220. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ CH₃ CH₃ 221. o,o′-diCH₃O-p-(CH═CHCN)phenyl F cyclopropyl CH₃ 222. o,o′-diCH₃O-p-(CH═CHCN)phenyl F cyclopropyl H 223. o,o′-diCH₃O-p-(CH═CHCN)phenyl F CH₃ H 224. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ CH₃ 225. 4-cyclopropylnaphth-1-yl SO₂NH₂ cyclopropyl CH₃ 226. 4-cyclopropylnaphth-1-yl SO₂NH₂ cyclopropyl H 227. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ H 228. 4-cyclopropylnaphth-1-yl F CH₃ CH₃ 229. 4-cyclopropylnaphth-1-yl F cyclopropyl CH₃ 230. 4-cyclopropylnaphth-1-yl F cyclopropyl H 231. 4-cyclopropylnaphth-1-yl F CH₃ H 232. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ CH₃ 233. o,o′-di-CH₃O-p-CN-phenyl SO₂NHCH₃ CH₃ CH₃ 234. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ cyclopropyl CH₃ 235. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ cyclopropyl H 236. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ H 237. o,o′-di-CH₃O-p-CN-phenyl F CH₃ CH₃ 238. o,o′-di-CH₃O-p-CN-phenyl F cyclopropyl CH₃ 239. o,o′-di-CH₃O-p-CN-phenyl F cyclopropyl H 240. o,o′-di-CH₃O-p-CN-phenyl F CH₃ H 241. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ CH₃ 242. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ cyclopropyl CH₃ 243. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ cyclopropyl H 244. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ H 245. o,o′-di-CH₃-p-CN-phenyl F CH₃ CH₃ 246. o,o′-di-CH₃-p-CN-phenyl F cyclopropyl CH₃ 247. o,o′-di-CH₃-p-CN-phenyl F cyclopropyl H 248. o,o′-di-CH₃-p-CN-phenyl F CH₃ H 249. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ CH₃ F 250. o,o′-diCH₃O-p-(CH═CHCN)phenyl SO₂NH₂ cyclopropyl F 251. o,o′-diCH₃O-p-(CH═CHCN)phenyl F cyclopropyl F 252. o,o′-diCH₃O-p-(CH═CHCN)phenyl F CH₃ F 253. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ F 254. 4-cyclopropylnaphth-1-yl SO₂NH₂ cyclopropyl F 255. 4-cyclopropylnaphth-1-yl F CH₃ F 256. 4-cyclopropylnaphth-1-yl F cyclopropyl F 257. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ F 258. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ cyclopropyl F 259. o,o′-di-CH₃O-p-CN-phenyl F CH₃ F 260. o,o′-di-CH₃O-p-CN-phenyl F cyclopropyl F 261. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ F 262. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ cyclopropyl F 263. o,o′-di-CH₃-p-CN-phenyl F CH₃ F 264. o,o′-di-CH₃-p-CN-phenyl F cyclopropyl F 265. 4-cyclopropyl phenyl CN CH₃ CH₃ 266. 2,4,6-trimethyl phenyl CN cyclopropyl CH₃ 267. 2,4,6-trimethyl phenyl CN cyclopropyl H 268. 2,4,6-trimethyl phenyl CN CH₃ H 269. 2,4,6-trimethyl phenyl CH═CHCN CH₃ CH₃ 270. 2,4,6-trimethyl phenyl CH═CHCN cyclopropyl CH₃ 271. 2,4,6-trimethyl phenyl CH═CHCN cyclopropyl H 272. 2,4,6-trimethyl phenyl CH═CHCN CH₃ H 273. 2,4,6-trimethyl phenyl CN CH₃ F 274. 2,4,6-trimethyl phenyl CN cyclopropyl F 275. 2,4,6-trimethyl phenyl CH═CHCN CH₃ F 276. 2,4,6-trimethyl phenyl CH═CHCN cyclopropyl F 277. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ CH₃ 278. 2,4,6-trimethyl phenyl SO₂NH₂ cyclopropyl CH₃ 279. 2,4,6-trimethyl phenyl SO₂NH₂ cyclopropyl H 280. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ H 281. 2,4,6-trimethyl phenyl F CH₃ CH₃ 282. 2,4,6-trimethyl phenyl F cyclopropyl CH₃ 283. 2,4,6-trimethyl phenyl F cyclopropyl H 284. 4-cyclopropyl phenyl F CH₃ H 285. 4-cyclopropyl phenyl SO₂NH₂ CH₃ F 286. 4-cyclopropyl phenyl SO₂NH₂ cyclopropyl F 287. 4-cyclopropyl phenyl F CH₃ F 288. 4-cyclopropyl phenyl F cyclopropyl F 289. 2,4,6-trimethyl phenyl CN CH₃ CH₃ 290. o,o′-dimethyl-p-cyclopropyl phenyl CN cyclopropyl CH₃ 291. o,o′-dimethyl-p-cyclopropyl phenyl CN cyclopropyl H 292. o,o′-dimethyl-p-cyclopropyl phenyl CN CH₃ H 293. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ CH₃ 294. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN cyclopropyl CH₃ 295. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN cyclopropyl H 296. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ H 297. o,o′-dimethyl-p-cyclopropyl phenyl CN CH₃ F 298. o,o′-dimethyl-p-cyclopropyl phenyl CN cyclopropyl F 299. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ F 300. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN cyclopropyl F 301. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ CH₃ 302. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ cyclopropyl CH₃ 303. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ cyclopropyl H 304. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ H 305. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ CH₃ 306. o,o′-dimethyl-p-cyclopropyl phenyl F cyclopropyl CH₃ 307. o,o′-dimethyl-p-cyclopropyl phenyl F cyclopropyl H 308. 2,4,6-trimethyl phenyl F CH₃ H 309. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ F 310. 2,4,6-trimethyl phenyl SO₂NH₂ cyclopropyl F 311. 2,4,6-trimethyl phenyl F CH₃ F 312. 2,4,6-trimethyl phenyl F cyclopropyl F 313. o,o′-di-CH₃-p-acetyl-phenyl CN CH₃ H 314. o,o′-di-CH₃-p-acetyl-phenyl CN H H 315. o,o′-di-CH₃-p-acetyl-phenyl CN CH₃ Cl 316. o,o′-di-CH₃-p-acetyl-phenyl CN H Cl

TABLE 2 Contemplated Compounds of Formula IA-2

Ar V W Z  1. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CN F CH₃  2. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CN benzyl CH₃  3. o,o′--diCH₃O-p-(CH═CHCN)-phenyl CN benzyl H  4. o,o′--diCH₃O-p-(CH═CHCN)-phenyl CN F H  5. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CH═CHCN Cl CH₃  6. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CH═CHCN benzyl CH₃  7. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CH═CHCN benzyl H  8. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CH═CHCN Cl H  9. 4-cyclopropylnaphth-1-yl C≡CCH₃ allyl ethyl  10. 4-cyclopropylnaphth-1-yl CN allyl ethyl  11. 4-cyclopropylnaphth-1-yl CN benzyl H  12. 4-cyclopropylnaphth-1-yl CN benzyl H  13. 4-cyclopropylnaphth-1-yl C≡CCH₃ allyl ethyl  14. 4-cyclopropylnaphth-1-yl CH═CHCN allyl ethyl  15. 4-cyclopropylnaphth-1-yl CH═CHCN 3-MeO-benzyl H  16. 4-cyclopropylnaphth-1-yl CH═CHCN benzyl H  17. o,o′-di-CH₃O-p-CN-phenyl SO₂NHCH₃ CH═CHCN CH₃  18. o,o′-di-CH₃O-p-CN-phenyl CN CH═CHCN CH₃  19. o,o′-di-CH₃O-p-CN-phenyl CN 3-Me-benzyl H  20. o,o′-di-CH₃O-p-CN-phenyl CN benzyl H  21. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH═CHCN CH₃  22. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₂CH₂CN CH₃  23. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₂CH₂CN H  24. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN benzyl H  25. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CN CH₃ H  26. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CN CH₃ benzyl  27. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CN H benzyl  28. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CN H H  29. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CH═CHCN CH₃ H  30. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CH═CHCN CH₃ benzyl  31. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CH═CHCN H benzyl  32. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CH═CHCN H H  33. 4-cyclopropylnaphth-1-yl CN CH₃ H  34. 4-cyclopropylnaphth-1-yl CN CH₃ benzyl  35. 4-cyclopropylnaphth-1-yl CN H benzyl  36. 4-cyclopropylnaphth-1-yl CN H H  37. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ H  38. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ benzyl  39. 4-cyclopropylnaphth-1-yl CH═CHCN H benzyl  40. 4-cyclopropylnaphth-1-yl CH═CHCN H H  41. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ H  42. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ benzyl  43. o,o′-di-CH₃O-p-CN-phenyl CN H benzyl  44. o,o′-di-CH₃O-p-CN-phenyl CN H H  45. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ H  46. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ benzyl  47. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H benzyl  48. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H H  49. o,o′-di-CH₃-p-CN-phenyl CN CH₃ H  50. o,o′-di-CH₃-p-CN-phenyl CN CH₃ benzyl  51. o,o′-di-CH₃-p-CN-phenyl CN H benzyl  52. o,o′-di-CH₃-p-CN-phenyl CN H H  53. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ H  54. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ benzyl  55. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H benzyl  56. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H H  57. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CN F H  58. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CN F benzyl  59. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CH═CHCN F benzyl  60. o,o′-di-CH₃O-p-(CH═CHCN)-phenyl CH═CHCN F H  61. 4-cyclopropylnaphth-1-yl CN F H  62. 4-cyclopropylnaphth-1-yl CN F benzyl  63. 4-cyclopropylnaphth-1-yl CH═CHCN F H  64. 4-cyclopropylnaphth-l-yl CH═CHCN F benzyl  65. o,o′-di-CH₃O-p-CN-phenyl CN F H  66. o,o′-di-CH₃O-p-CN-phenyl CN F benzyl  67. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN F H  68. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN F benzyl  69. o,o′-di-CH₃-p-CN-phenyl CN F H  70. o,o′-di-CH₃-p-CN-phenyl CN F benzyl  71. o,o′-di-CH₃-p-CN-phenyl CH═CHCN F H  72. o,o′-di-CH₃-p-CN-phenyl CH═CHCN F benzyl  73. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ CH₃ H  74. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ CH₃ benzyl  75. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ H benzyl  76. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ H H  77. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ CH₃ H  78. o,o′-diCH₃O-p-(CH═CHCN)-phenyl F CH₃ benzyl  79. o,o′-diCH₃O-p-(CH═CHCN)-phenyl F H benzyl  80. o,o′-diCH₃O-p-(CH═CHCN)-phenyl F H H  81. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ H  82. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ benzyl  83. 4-cyclopropylnaphth-1-yl SO₂NH₂ H benzyl  84. 4-cyclopropylnaphth-1-yl SO₂NH₂ H H  85. 4-cyclopropylnaphth-1-yl F CH₃ H  86. 4-cyclopropylnaphth-1-yl F CH₃ benzyl  87. 4-cyclopropylnaphth-1-yl F H benzyl  88. 4-cyclopropylnaphth-1-yl F H H  89. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ H  90. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ benzyl  91. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H benzyl  92. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H H  93. o,o′-di-CH₃O-p-CN-phenyl F CH₃ H  94. o,o′-di-CH₃O-p-CN-phenyl F CH₃ benzyl  95. o,o′-di-CH₃O-p-CN-phenyl F H benzyl  96. o,o′-di-CH₃O-p-CN-phenyl F H H  97. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ H  98. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ benzyl  99. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H benzyl 100. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H H 101. o,o′-di-CH₃-p-CN-phenyl F CH₃ H 102. o,o′-di-CH₃-p-CN-phenyl F CH₃ benzyl 103. o,o′-di-CH₃-p-CN-phenyl F H benzyl 104. o,o′-di-CH₃-p-CN-phenyl F H H 105. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ F H 106. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ F benzyl 107. o,o′-diCH₃O-p-(CH═CHCN)-phenyl F F benzyl 108. o,o′-diCH₃O-p-(CH═CHCN)-phenyl F F H 109. 4-cyclopropylnaphth-1-yl SO₂NH₂ F H 110. 4-cyclopropylnaphth-1-yl SO₂NH₂ F benzyl 111. 4-cyclopropylnaphth-1-yl F F H 112. 4-cyclopropylnaphth-1-yl F F benzyl 113. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ F H 114. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ F benzyl 115. o,o′-di-CH₃O-p-CN-phenyl F F H 116. o,o′-di-CH₃O-p-CN-phenyl F F benzyl 117. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ F H 118. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ F benzyl 119. o,o′-di-CH₃-p-CN-phenyl F F H 120. o,o′-di-CH₃-p-CN-phenyl F F benzyl 121. 4-cyclopropyl phenyl CN CH₃ H 122. 4-cyclopropyl phenyl CN CH₃ benzyl 123. 4-cyclopropyl phenyl CN H benzyl 124. 4-cyclopropyl phenyl CN H H 125. 2,4,6-trimethyl phenyl CH═CHCN CH₃ H 126. 2,4,6-trimethyl phenyl CH═CHCN CH₃ benzyl 127. 2,4,6-trimethyl phenyl CH═CHCN H benzyl 128. 2,4,6-trimethyl phenyl CH═CHCN H H 129. 2,4,6-trimethyl phenyl CN F H 130. 2,4,6-trimethyl phenyl CN F benzyl 131. 2,4,6-trimethyl phenyl CH═CHCN F H 132. 2,4,6-trimethyl phenyl CH═CHCN F benzyl 133. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ H 134. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ benzyl 135. 2,4,6-trimethyl phenyl SO₂NH₂ H benzyl 136. 2,4,6-trimethyl phenyl SO₂NH₂ H H 137. 2,4,6-trimethyl phenyl F CH₃ H 138. 2,4,6-trimethyl phenyl F CH₃ benzyl 139. 2,4,6-trimethyl phenyl F H benzyl 140. 4-cyclopropyl phenyl F H H 141. 4-cyclopropyl phenyl SO₂NH₂ F H 142. 4-cyclopropyl phenyl SO₂NH₂ F benzyl 143. 4-cyclopropyl phenyl F F H 144. 4-cyclopropyl phenyl F F benzyl 145. o,o′-dimethyl-p-cyclopropyl phenyl CN CH₃ H 146. o,o′-dimethyl-p-cyclopropyl phenyl CN CH₃ benzyl 147. o,o′-dimethyl-p-cyclopropyl phenyl CN H benzyl 148. o,o′-dimethyl-p-cyclopropyl phenyl CN H H 149. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ H 150. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ benzyl 151. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H benzyl 152. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H H 153. o,o′-dimethyl-p-cyclopropyl phenyl CN F H 154. o,o′-dimethyl-p-cyclopropyl phenyl CN F benzyl 155. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN F H 156. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN F benzyl 157. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ H 158. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ benzyl 159. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H benzyl 160. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H H 161. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ H 162. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ benzyl 163. o,o′-dimethyl-p-cyclopropyl phenyl F H benzyl 164. o,o′-dimethyl-p-cyclopropyl phenyl F H H 165. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ F H 166. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ F benzyl 167. 2-methyl-4-cyclopropyl phenyl F F H 168. 2-methyl-4-cyclopropyl phenyl F F benzyl 169. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CN CH₃ CH₃ 170. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CN CH₃ cyclopropyl 171. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CN H cyclopropyl 172. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CN H CH₃ 173. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CH═CHCN CH₃ CH₃ 174. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CH═CHCN CH₃ cyclopropyl 175. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CH═CHCN H cyclopropyl 176. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CH═CHCN H CH₃ 177. 4-cyclopropylnaphth-1-yl CN CH₃ CH₃ 178. 4-cyclopropylnaphth-1-yl CN CH₃ cyclopropyl 179. 4-cyclopropylnaphth-1-yl CN H cyclopropyl 180. 4-cyclopropylnaphth-1-yl CN H CH₃ 181. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ CH₃ 182. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ cyclopropyl 183. 4-cyclopropylnaphth-1-yl CH═CHCN H cyclopropyl 184. 4-cyclopropylnaphth-1-yl CH═CHCN H CH₃ 185. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ CH₃ 186. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ cyclopropyl 187. o,o′-di-CH₃O-p-CN-phenyl CN H cyclopropyl 188. o,o′-di-CH₃O-p-CN-phenyl CN H CH₃ 189. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ CH₃ 190. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ cyclopropyl 191. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H cyclopropyl 192. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H CH₃ 193. o,o′-di-CH₃-p-CN-phenyl CN CH₃ CH₃ 194. o,o′-di-CH₃-p-CN-phenyl CN CH₃ cyclopropyl 195. o,o′-di-CH₃-p-CN-phenyl CN H cyclopropyl 196. o,o′-di-CH₃-p-CN-phenyl CN H CH₃ 197. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ CH₃ 198. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ cyclopropyl 199. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H cyclopropyl 200. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H CH₃ 201. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CN F CH₃ 202. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CN F cyclopropyl 203. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CH═CHCN F cyclopropyl 204. o,o′-diCH₃O-p-(CH═CHCN)-phenyl CH═CHCN F CH₃ 205. 4-cyclopropylnaphth-1-yl CN F CH₃ 206. 4-cyclopropylnaphth-1-yl CN F cyclopropyl 207. 4-cyclopropylnaphth-1-yl CH═CHCN F CH₃ 208. 4-cyclopropylnaphth-1-yl CH═CHCN F cyclopropyl 209. o,o′-di-CH₃O-p-CN-phenyl CN F CH₃ 210. o,o′-di-CH₃O-p-CN-phenyl CN F cyclopropyl 211. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN F CH₃ 212. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN F cyclopropyl 213. o,o′-di-CH₃-p-CN-phenyl CN F CH₃ 214. o,o′-di-CH₃-p-CN-phenyl CN F cyclopropyl 215. o,o′-di-CH₃-p-CN-phenyl CH═CHCN F CH₃ 216. o,o′-di-CH₃-p-CN-phenyl CH═CHCN F cyclopropyl 217. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ CH₃ CH₃ 218. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ CH₃ cyclopropyl 219. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ H cyclopropyl 220. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ H CH₃ 221. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ CH₃ CH₃ 222. o,o′-diCH₃O-p-(CH═CHCN)-phenyl F CH₃ cyclopropyl 223. o,o′-diCH₃O-p-(CH═CHCN)-phenyl F H cyclopropyl 224. o,o′-diCH₃O-p-(CH═CHCN)-phenyl F H CH₃ 225. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ CH₃ 226. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ cyclopropyl 227. 4-cyclopropylnaphth-1-yl SO₂NH₂ H cyclopropyl 228. 4-cyclopropylnaphth-1-yl SO₂NH₂ H CH₃ 229. 4-cyclopropylnaphth-1-yl F CH₃ CH₃ 230. 4-cyclopropylnaphth-1-yl F CH₃ cyclopropyl 231. 4-cyclopropylnaphth-1-yl F H cyclopropyl 232. 4-cyclopropylnaphth-1-yl F H CH₃ 233. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ CH₃ 234. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ cyclopropyl 235. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H cyclopropyl 236. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H CH₃ 237. o,o′-di-CH₃O-p-CN-phenyl F CH₃ CH₃ 238. o,o′-di-CH₃O-p-CN-phenyl F CH₃ cyclopropyl 239. o,o′-di-CH₃O-p-CN-phenyl F H cyclopropyl 240. o,o′-di-CH₃O-p-CN-phenyl F H CH₃ 241. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ CH₃ 242. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ cyclopropyl 243. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H cyclopropyl 244. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H CH₃ 245. o,o′-di-CH₃-p-CN-phenyl F CH₃ CH₃ 246. o,o′-di-CH₃-p-CN-phenyl F CH₃ cyclopropyl 247. o,o′-di-CH₃-p-CN-phenyl F H cyclopropyl 248. o,o′-di-CH₃-p-CN-phenyl F H CH₃ 249. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ F CH₃ 250. o,o′-diCH₃O-p-(CH═CHCN)-phenyl SO₂NH₂ F cyclopropyl 251. o,o′-diCH₃O-p-(CH═CHCN)-phenyl F F cyclopropyl 252. o,o′-diCH₃O-p-(CH═CHCN)-phenyl F F CH₃ 253. 4-cyclopropylnaphth-1-yl SO₂NH₂ F CH₃ 254. 4-cyclopropylnaphth-1-yl SO₂NH₂ F cyclopropyl 255. 4-cyclopropylnaphth-1-yl F F CH₃ 256. 4-cyclopropylnaphth-1-yl F F cyclopropyl 257. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ F CH₃ 258. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ F cyclopropyl 259. o,o′-di-CH₃O-p-CN-phenyl F F CH₃ 260. o,o′-di-CH₃O-p-CN-phenyl F F cyclopropyl 261. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ F CH₃ 262. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ F cyclopropyl 263. o,o′-di-CH₃-p-CN-phenyl F F CH₃ 264. o,o′-di-CH₃-p-CN-phenyl F F cyclopropyl 265. 4-cyclopropyl phenyl CN CH₃ CH₃ 266. 2,4,6-trimethyl phenyl CN CH₃ cyclopropyl 267. 2,4,6-trimethyl phenyl CN H cyclopropyl 268. 2,4,6-trimethyl phenyl CN H CH₃ 269. 2,4,6-trimethyl phenyl CH═CHCN CH₃ CH₃ 270. 2,4,6-trimethyl phenyl CH═CHCN CH₃ cyclopropyl 271. 2,4,6-trimethyl phenyl CH═CHCN H cyclopropyl 272. 2,4,6-trimethyl phenyl CH═CHCN H CH₃ 273. 2,4,6-trimethyl phenyl CN F CH₃ 274. 2,4,6-trimethyl phenyl CN F cyclopropyl 275. 2,4,6-trimethyl phenyl CH═CHCN F CH₃ 276. 2,4,6-trimethyl phenyl CH═CHCN F cyclopropyl 277. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ CH₃ 278. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ cyclopropyl 279. 2,4,6-trimethyl phenyl SO₂NH₂ H cyclopropyl 280. 2,4,6-trimethyl phenyl SO₂NH₂ H CH₃ 281. 2,4,6-trimethyl phenyl F CH₃ CH₃ 282. 2,4,6-trimethyl phenyl F CH₃ cyclopropyl 283. 2,4,6-trimethyl phenyl F H cyclopropyl 284. 2,4,6-trimethyl phenyl F H CH₃ 285. 2,4,6-trimethyl phenyl SO₂NH₂ F CH₃ 286. 4-cyclopropyl phenyl SO₂NH₂ F cyclopropyl 287. 4-cyclopropyl phenyl F F CH₃ 288. 4-cyclopropyl phenyl F F cyclopropyl 289. o,o′-dimethyl-p-cyclopropyl phenyl CN CH₃ CH₃ 290. o,o′-dimethyl-p-cyclopropyl phenyl CN CH₃ cyclopropyl 291. o,o′-dimethyl-p-cyclopropyl phenyl CN H cyclopropyl 292. o,o′-dimethyl-p-cyclopropyl phenyl CN H CH₃ 293. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ CH₃ 294. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ cyclopropyl 295. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H cyclopropyl 296. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H CH₃ 297. o,o′-dimethyl-p-cyclopropyl phenyl CN F CH₃ 298. o,o′-dimethyl-p-cyclopropyl phenyl CN F cyclopropyl 299. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN F CH₃ 300. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN F cyclopropyl 301. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ CH₃ 302. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ cyclopropyl 303. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H cyclopropyl 304. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H CH₃ 305. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ CH₃ 306. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ cyclopropyl 307. o,o′-dimethyl-p-cyclopropyl phenyl F H cyclopropyl 308. o,o′-dimethyl-p-cyclopropyl phenyl F H CH₃ 309. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ F CH₃ 310. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ F cyclopropyl 311. o,o′-dimethyl-p-cyclopropyl phenyl F F CH₃ 312. o,o′-dimethyl-p-cyclopropyl phenyl F F cyclopropyl 313. o,o′-di-CH₃-p-acetyl-phenyl CN H H 314. o,o′-di-CH₃-p-acetyl-phenyl CN CH₃ H 315. o,o′-di-CH₃-p-acetyl-phenyl CN H Cl 316. o,o′-di-CH₃-p-acetyl-phenyl CN CH₃ Cl

TABLE 3 Contemplated Compounds of Formula IA-3

Ar V W Z  1. o,o′-diCH₃O-p-(CH═CHCN)- CN benzyl F phenyl  2. o,o′-diCH₃O-p-(CH═CHCN)- CN benzyl Cl phenyl  3. o,o′-diCH₃O-p-(CH═CHCN)- CN allyl F phenyl  4. o,o′-diCH₃O-p-(CH═CHCN)- CN allyl Cl phenyl  5. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN benzyl CH₃ phenyl  6. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN 3-MeO- CH₃ phenyl benzyl  7. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN 3-Me- CH₃ phenyl benzyl  8. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN allyl CH₃ phenyl  9. 4-cyclopropylnaphth-1-yl CN CH₂CH₃ H  10. 4-cyclopropylnaphth-1-yl CN isopropyl H  11. 4-cyclopropylnaphth-1-yl CN CH₂CF₃ Br  12. 4-cyclopropylnaphth-1-yl CN CH₂CF₃ Cl  13. 4-cyclopropylnaphth-1-yl CH═CHCN CH₂CH₃ H  14. 4-cyclopropylnaphth-1-yl CH═CHCN CH₂CH₃ Br  15. 4-cyclopropylnaphth-1-yl CH═CHCN CH₂CF₃ CH₃  16. 4-cyclopropylnaphth-1-yl CH═CHCN CH₂CF₃ H  17. o,o′-di-CH₃O-p-CN-phenyl CN benzyl F  18. o,o′-di-CH₃O-p-CN-phenyl CN benzyl Cl  19. o,o′-di-CH₃O-p-CN-phenyl CN allyl F  20. o,o′-di-CH₃O-p-CN-phenyl CN allyl Cl  21. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN benzyl CH₃  22. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN benzyl Br  23. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN allyl CH₃  24. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN allyl H  25. o,o′-diCH₃O-p-(CH═CHCN)- CN H F phenyl  26. o,o′-diCH₃O-p-(CH═CHCN)- CN benzyl Cl phenyl  27. o,o′-diCH₃O-p-(CH═CHCN)- CN benzyl H phenyl  28. o,o′-diCH₃O-p-(CH═CHCN)- CN H H phenyl  29. o,o′-diCH₃O-p-(CH═CHCN)- CN H CH₃ phenyl  30. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN benzyl CH₃ phenyl  31. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN benzyl H phenyl  32. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN H H phenyl  33. 4-cyclopropylnaphth-1-yl CN H CH₃  34. 4-cyclopropylnaphth-1-yl CN benzyl CH₃  35. 4-cyclopropylnaphth-1-yl CN benzyl H  36. 4-cyclopropylnaphth-1-yl CN H H  37. 4-cyclopropylnaphth-1-yl CH═CHCN H CH₃  38. 4-cyclopropylnaphth-1-yl CH═CHCN benzyl CH₃  39. 4-cyclopropylnaphth-1-yl CH═CHCN benzyl H  40. 4-cyclopropylnaphth-1-yl CH═CHCN H H  41. o,o′-di-CH₃O-p-CN-phenyl CN H CH₃  42. o,o′-di-CH₃O-p-CN-phenyl CN benzyl CH₃  43. o,o′-di-CH₃O-p-CN-phenyl CN benzyl H  44. o,o′-di-CH₃O-p-CN-phenyl CN H H  45. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H CH₃  46. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN benzyl CH₃  47. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN benzyl H  48. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H H  49. o,o′-di-CH₃-p-CN-phenyl CN H CH₃  50. o,o′-di-CH₃-p-CN-phenyl CN benzyl CH₃  51. o,o′-di-CH₃-p-CN-phenyl CN benzyl H  52. o,o′-di-CH₃-p-CN-phenyl CN H H  53. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H CH₃  54. o,o′-di-CH₃-p-CN-phenyl CH═CHCN benzyl CH₃  55. o,o′-di-CH₃-p-CN-phenyl CH═CHCN benzyl H  56. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H H  57. o,o′-diCH₃O-p-(CH═CHCN)- CN H F phenyl  58. o,o′-diCH₃O-p-(CH═CHCN)- CN benzyl F phenyl  59. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN benzyl F phenyl  60. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN H F phenyl  61. 4-cyclopropylnaphth-1-yl CN H F  62. 4-cyclopropylnaphth-1-yl CN benzyl F  63. 4-cyclopropylnaphth-1-yl CH═CHCN H F  64. 4-cyclopropylnaphth-1-yl CH═CHCN benzyl F  65. o,o′-di-CH₃O-p-CN-phenyl CN H F  66. o,o′-di-CH₃O-p-CN-phenyl CN benzyl F  67. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H F  68. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN benzyl F  69. o,o′-di-CH₃-p-CN-phenyl CN H F  70. o,o′-di-CH₃-p-CN-phenyl CN benzyl F  71. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H F  72. o,o′-di-CH₃-p-CN-phenyl CH═CHCN benzyl F  73. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ H CH₃ phenyl  74. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ benzyl CH₃ phenyl  75. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ benzyl H phenyl  76. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ H H phenyl  77. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ H CH₃ phenyl  78. o,o′-diCH₃O-p-(CH═CHCN)- F benzyl CH₃ phenyl  79. o,o′-diCH₃O-p-(CH═CHCN)- F benzyl H phenyl  80. o,o′-diCH₃O-p-(CH═CHCN)- F H H phenyl  81. 4-cyclopropylnaphth-1-yl SO₂NH₂ H CH₃  82. 4-cyclopropylnaphth-1-yl SO₂NH₂ benzyl CH₃  83. 4-cyclopropylnaphth-1-yl SO₂NH₂ benzyl H  84. 4-cyclopropylnaphth-1-yl SO₂NH₂ H H  85. 4-cyclopropylnaphth-1-yl F H CH₃  86. 4-cyclopropylnaphth-1-yl F benzyl CH₃  87. 4-cyclopropylnaphth-1-yl F benzyl H  88. 4-cyclopropylnaphth-1-yl F H H  89. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H CH₃  90. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ benzyl CH₃  91. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ benzyl H  92. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H H  93. o,o′-di-CH₃O-p-CN-phenyl F H CH₃  94. o,o′-di-CH₃O-p-CN-phenyl F benzyl CH₃  95. o,o′-di-CH₃O-p-CN-phenyl F benzyl H  96. o,o′-di-CH₃O-p-CN-phenyl F H H  97. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H CH₃  98. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ benzyl CH₃  99. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ benzyl H 100. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H H 101. o,o′-di-CH₃-p-CN-phenyl F H CH₃ 102. o,o′-di-CH₃-p-CN-phenyl F benzyl CH₃ 103. o,o′-di-CH₃-p-CN-phenyl F benzyl H 104. o,o′-di-CH₃-p-CN-phenyl F H H 105. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ H F phenyl 106. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ benzyl F phenyl 107. o,o′-diCH₃O-p-(CH═CHCN)- F benzyl F phenyl 108. o,o′-diCH₃O-p-(CH═CHCN)- F H F phenyl 109. 4-cyclopropylnaphth-1-yl SO₂NH₂ H F 110. 4-cyclopropylnaphth-1-yl SO₂NH₂ benzyl F 111. 4-cyclopropylnaphth-1-yl F H F 112. 4-cyclopropylnaphth-1-yl F benzyl F 113. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H F 114. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ benzyl F 115. o,o′-di-CH₃O-p-CN-phenyl F H F 116. o,o′-di-CH₃O-p-CN-phenyl F benzyl F 117. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H F 118. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ benzyl F 119. o,o′-di-CH₃-p-CN-phenyl F H F 120. o,o′-di-CH₃-p-CN-phenyl F benzyl F 121. 2,4,6-trimethyl phenyl CN H CH₃ 122. 2,4,6-trimethyl phenyl CN benzyl CH₃ 123. 2,4,6-trimethyl phenyl CN benzyl H 124. 2,4,6-trimethyl phenyl CN H H 125. 2,4,6-trimethyl phenyl CH═CHCN H CH₃ 126. 2,4,6-trimethyl phenyl CH═CHCN benzyl CH₃ 127. 4-cyclopropyl phenyl CH═CHCN benzyl H 128. 4-cyclopropyl phenyl CH═CHCN H H 129. 4-cyclopropyl phenyl CN H F 130. 4-cyclopropyl phenyl CN benzyl F 131. 4-cyclopropyl phenyl CH═CHCN H F 132. 2,4,6-trimethyl phenyl CH═CHCN benzyl F 133. 2,4,6-trimethyl phenyl SO₂NH₂ H CH₃ 134. 2,4,6-trimethyl phenyl SO₂NH₂ benzyl CH₃ 135. 2,4,6-trimethyl phenyl SO₂NH₂ benzyl H 136. 2,4,6-trimethyl phenyl SO₂NH₂ H H 137. 2,4,6-trimethyl phenyl F H CH₃ 138. 2,4,6-trimethyl phenyl F benzyl CH₃ 139. 2,4,6-trimethyl phenyl F benzyl H 140. 2,4,6-trimethyl phenyl F H H 141. 2,4,6-trimethyl phenyl SO₂NH₂ H F 142. 2,4,6-trimethyl phenyl SO₂NH₂ benzyl F 143. 2,4,6-trimethyl phenyl F H F 144. 2,4,6-trimethyl phenyl F benzyl F 145. 2,4,6-trimethyl phenyl CN H CH₃ 146. 2,4,6-trimethyl phenyl CN benzyl CH₃ 147. 2,4,6-trimethyl phenyl CN benzyl H 148. 2,4,6-trimethyl phenyl CN H H 149. 2,4,6-trimethyl phenyl CH═CHCN H CH₃ 150. 2,4,6-trimethyl phenyl CH═CHCN benzyl CH₃ 151. 2,4,6-trimethyl phenyl CH═CHCN benzyl H 152. 2,4,6-trimethyl phenyl CH═CHCN H H 153. 2,4,6-trimethyl phenyl CN H F 154. 2,4,6-trimethyl phenyl CN benzyl F 155. 2,4,6-trimethyl phenyl CH═CHCN H F 156. 2,4,6-trimethyl phenyl CH═CHCN benzyl F 157. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H CH₃ 158. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ benzyl CH₃ 159. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ benzyl H 160. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H H 161. o,o′-dimethyl-p-cyclopropyl phenyl F H CH₃ 162. o,o′-dimethyl-p-cyclopropyl phenyl F benzyl CH₃ 163. o,o′-dimethyl-p-cyclopropyl phenyl F benzyl H 164. o,o′-dimethyl-p-cyclopropyl phenyl F H H 165. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H F 166. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ benzyl F 167. o,o′-dimethyl-p-cyclopropyl phenyl F H F 168. o,o′-dimethyl-p-cyclopropyl phenyl F benzyl F 169. o,o′-diCH₃O-p-(CH═CHCN)- CN CH₃ CH₃ phenyl 170. o,o′-diCH₃O-p-(CH═CHCN)- CN cyclo- CH₃ phenyl propyl 171. o,o′-diCH₃O-p-(CH═CHCN)- CN cyclo- H phenyl propyl 172. o,o′-diCH₃O-p-(CH═CHCN)- CN CH₃ H phenyl 173. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN CH₃ CH₃ phenyl 174. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN cyclo- CH₃ phenyl propyl 175. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN cyclo- H phenyl propyl 176. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN CH₃ H phenyl 177. 4-cyclopropylnaphth-1-yl CN CH₃ CH₃ 178. 4-cyclopropylnaphth-1-yl CN cyclo- CH₃ propyl 179. 4-cyclopropylnaphth-1-yl CN cyclo- H propyl 180. 4-cyclopropylnaphth-1-yl CN CH₃ H 181. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ CH₃ 182. 4-cyclopropylnaphth-1-yl CH═CHCN cyclo- CH₃ propyl 183. 4-cyclopropylnaphth-1-yl CH═CHCN cyclo- H propyl 184. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ H 185. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ CH₃ 186. o,o′-di-CH₃O-p-CN-phenyl CN cyclo- CH₃ propyl 187. o,o′-di-CH₃O-p-CN-phenyl CN cyclo- H propyl 188. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ H 189. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ CH₃ 190. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN cyclo- CH₃ propyl 191. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN cyclo- H propyl 192. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ H 193. o,o′-di-CH₃-p-CN-phenyl CN CH₃ CH₃ 194. o,o′-di-CH₃-p-CN-phenyl CN cyclo- CH₃ propyl 195. o,o′-di-CH₃-p-CN-phenyl CN cyclo- H propyl 196. o,o′-di-CH₃-p-CN-phenyl CN CH₃ H 197. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ CH₃ 198. o,o′-di-CH₃-p-CN-phenyl CH═CHCN cyclo- CH₃ propyl 199. o,o′-di-CH₃-p-CN-phenyl CH═CHCN cyclo- H propyl 200. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ H 201. o,o′-diCH₃O-p-(CH═CHCN)- CN CH₃ F phenyl 202. o,o′-diCH₃O-p-(CH═CHCN)- CN cyclo- F phenyl propyl 203. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN cyclo- F phenyl propyl 204. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN CH₃ F phenyl 205. 4-cyclopropylnaphth-1-yl CN CH₃ F 206. 4-cyclopropylnaphth-1-yl CN cyclo- F propyl 207. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ F 208. 4-cyclopropylnaphth-1-yl CH═CHCN cyclo- F propyl 209. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ F 210. o,o′-di-CH₃O-p-CN-phenyl CN cyclo- F propyl 211. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ F 212. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN cyclo- F propyl 213. o,o′-di-CH₃-p-CN-phenyl CN CH₃ F 214. o,o′-di-CH₃-p-CN-phenyl CN cyclo- F propyl 215. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ F 216. o,o′-di-CH₃-p-CN-phenyl CH═CHCN cyclo- F propyl 217. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ CH₃ CH₃ phenyl 218. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ cyclo- CH₃ phenyl propyl 219. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ cyclo- H phenyl propyl 220. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ CH₃ H phenyl 221. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ CH₃ CH₃ phenyl 222. o,o′-diCH₃O-p-(CH═CHCN)- F cyclo- CH₃ phenyl propyl 223. o,o′-diCH₃O-p-(CH═CHCN)- F cyclo- H phenyl propyl 224. o,o′-diCH₃O-p-(CH═CHCN)- F CH₃ H phenyl 225. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ CH₃ 226. 4-cyclopropylnaphth-1-yl SO₂NH₂ cyclo- CH₃ propyl 227. 4-cyclopropylnaphth-1-yl SO₂NH₂ cyclo- H propyl 228. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ H 229. 4-cyclopropylnaphth-1-yl F CH₃ CH₃ 230. 4-cyclopropylnaphth-1-yl F cyclo- CH₃ propyl 231. 4-cyclopropylnaphth-1-yl F cyclo- H propyl 232. 4-cyclopropylnaphth-1-yl F CH₃ H 233. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ CH₃ 234. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ cyclo- CH₃ propyl 235. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ cyclo- H propyl 236. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ H 237. o,o′-di-CH₃O-p-CN-phenyl F CH₃ CH₃ 238. o,o′-di-CH₃O-p-CN-phenyl F cyclo- CH₃ propyl 239. o,o′-di-CH₃O-p-CN-phenyl F cyclo- H propyl 240. o,o′-di-CH₃O-p-CN-phenyl F CH₃ H 241. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ CH₃ 242. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ cyclo- CH₃ propyl 243. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ cyclo- H propyl 244. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ H 245. o,o′-di-CH₃-p-CN-phenyl F CH₃ CH₃ 246. o,o′-di-CH₃-p-CN-phenyl F cyclo- CH₃ propyl 247. o,o′-di-CH₃-p-CN-phenyl F cyclo- H propyl 248. o,o′-di-CH₃-p-CN-phenyl F CH₃ H 249. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ CH₃ F phenyl 250. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ cyclo- F phenyl propyl 251. o,o′-diCH₃O-p-(CH═CHCN)- F cyclo- F phenyl propyl 252. o,o′-diCH₃O-p-(CH═CHCN)- F CH₃ F phenyl 253. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ F 254. 4-cyclopropylnaphth-1-yl SO₂NH₂ cyclo- F propyl 255. 4-cyclopropylnaphth-1-yl F CH₃ F 256. 4-cyclopropylnaphth-1-yl F cyclo- F propyl 257. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ F 258. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ cyclo- F propyl 259. o,o′-di-CH₃O-p-CN-phenyl F CH₃ F 260. o,o′-di-CH₃O-p-CN-phenyl F cyclo- F propyl 261. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ F 262. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ cyclo- F propyl 263. o,o′-di-CH₃-p-CN-phenyl F CH₃ F 264. o,o′-di-CH₃-p-CN-phenyl F cyclo- F propyl 265. 4-cyclopropyl phenyl CN CH₃ CH₃ 266. 4-cyclopropyl phenyl CN cyclo- CH₃ propyl 267. 2,4,6-trimethyl phenyl CN cyclo- H propyl 268. 2,4,6-trimethyl phenyl CN CH₃ H 269. 2,4,6-trimethyl phenyl CH═CHCN CH₃ CH₃ 270. 2,4,6-trimethyl phenyl CH═CHCN cyclo- CH₃ propyl 271. 2,4,6-trimethyl phenyl CH═CHCN cyclo- H propyl 272. 2,4,6-trimethyl phenyl CH═CHCN CH₃ H 273. 2,4,6-trimethyl phenyl CN CH₃ F 274. 2,4,6-trimethyl phenyl CN cyclo- F propyl 275. 2,4,6-trimethyl phenyl CH═CHCN CH₃ F 276. 2,4,6-trimethyl phenyl CH═CHCN cyclo- F propyl 277. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ CH₃ 278. 2,4,6-trimethyl phenyl SO₂NH₂ cyclo- CH₃ propyl 279. 2,4,6-trimethyl phenyl SO₂NH₂ cyclo- H propyl 280. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ H 281. 2,4,6-trimethyl phenyl F CH₃ CH₃ 282. 2,4,6-trimethyl phenyl F cyclo- CH₃ propyl 283. 2,4,6-trimethyl phenyl F cyclo- H propyl 284. 2,4,6-trimethyl phenyl F CH₃ H 285. 4-cyclopropyl phenyl SO₂NH₂ CH₃ F 286. 4-cyclopropyl phenyl SO₂NH₂ cyclo- F propyl 287. 4-cyclopropyl phenyl F CH₃ F 288. 4-cyclopropyl phenyl F cyclo- F propyl 289. 2,4,6-trimethyl phenyl CN CH₃ CH₃ 290. 2,4,6-trimethyl phenyl CN cyclo- CH₃ propyl 291. o,o′-dimethyl-p-cyclopropyl phenyl CN cyclo- H propyl 292. o,o′-dimethyl-p-cyclopropyl phenyl CN CH₃ H 293. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ CH₃ 294. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN cyclo- CH₃ propyl 295. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN cyclo- H propyl 296. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ H 297. o,o′-dimethyl-p-cyclopropyl phenyl CN CH₃ F 298 o,o′-dimethyl-p-cyclopropyl phenyl CN cyclo- F propyl 299. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ F 300. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN cyclo- F propyl 301. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ CH₃ 302. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ cyclo- CH₃ propyl 303. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ cyclo- H propyl 304. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ H 305. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ CH₃ 306. o,o′-dimethyl-p-cyclopropyl phenyl F cyclo- CH₃ propyl 307. o,o′-dimethyl-p-cyclopropyl phenyl F cyclo- H propyl 308. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ H 309. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ F 310. 2,4,6-trimethyl phenyl SO₂NH₂ cyclo- F propyl 311. 2,4,6-trimethyl phenyl F CH₃ F 312. 2,4,6-trimethyl phenyl F cyclo- F propyl 313. o,o′-di-CH₃-p-acetyl-phenyl CN H H 314. o,o′-di-CH₃-p-acetyl-phenyl CN CH₃ H 315. o,o′-di-CH₃-p-acetyl-phenyl CN H Cl 316. o,o′-di-CH₃-p-acetyl-phenyl CN CH₃ Cl

TABLE 4 Contemplated Compounds of Formula IA-4

Ar V W Z  1. o,o′-diCH₃O-p-(CH═CHCN)- CN H H phenyl  2. o,o′-diCH₃O-p-(CH═CHCN)- CN CH₃ H phenyl  3. o,o′-diCH₃O-p-(CH═CHCN)- CN F CH₃ phenyl  4. o,o′-diCH₃O-p-(CH═CHCN)- CN Cl CH₃ phenyl  5. o,o′-diCH₃O-p-(CH═CHCN)- CN F H phenyl  6. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN Cl H phenyl  7. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN Br CH₃ phenyl  8. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN H CH₃ phenyl  9. 4-cyclopropylnaphth-1-yl CN H H  10. 4-cyclopropylnaphth-1-yl CN CH₃ H  11. 4-cyclopropylnaphth-1-yl CN F CH₃  12. 4-cyclopropylnaphth-1-yl CN Cl CH₃  13. 4-cyclopropylnaphth-1-yl CH═CHCN Cl H  14. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ H  15. 4-cyclopropylnaphth-1-yl CH═CHCN F CH₃  16. 4-cyclopropylnaphth-1-yl CH═CHCN Cl CH₃  17. o,o′-di-CH₃O-p-CN-phenyl CN Br H  18. o,o′-di-CH₃O-p-CN-phenyl CN H H  19. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ CH₃  20. o,o′-di-CH₃O-p-CN-phenyl CN F CH₃  21. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H H  22. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ H  23. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN F CH₃  24. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN Cl CH₃  25. o,o′-diCH₃O-p-(CH═CHCN)- CN F CH₃ phenyl  26. o,o′-diCH₃O-p-(CH═CHCN)- CN Cl CH₃ phenyl  27. o,o′-diCH₃O-p-(CH═CHCN)- CN Cl H phenyl  28. o,o′-diCH₃O-p-(CH═CHCN)- CN F H phenyl  29. o,o′-diCH₃O-p-(CH═CHCN)- CN H CH₃ phenyl  30. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN CH₃ CH₃ phenyl  31. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN F H phenyl  32. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN Cl H phenyl  33. 4-cyclopropylnaphth-1-yl CN H ethyl  34. 4-cyclopropylnaphth-1-yl CN Cl ethyl  35. 4-cyclopropylnaphth-1-yl CN F H  36. 4-cyclopropylnaphth-1-yl CN Cl H  37. 4-cyclopropylnaphth-1-yl CH═CHCN Br ethyl  38. 4-cyclopropylnaphth-1-yl CH═CHCN H ethyl  39. 4-cyclopropylnaphth-1-yl CH═CHCN H H  40. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ H  41. o,o′-di-CH₃O-p-CN-phenyl CN F CH₃  42. o,o′-di-CH₃O-p-CN-phenyl CN Cl CH₃  43. o,o′-di-CH₃O-p-CN-phenyl CN Cl H  44. o,o′-di-CH₃O-p-CN-phenyl CN F H  45. o,o′-di-CH₃O-p-CN-phenyl C≡CCH₃ Cl CH₃  46. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN Br CH₃  47. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN Br H  48. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H H  49. o,o′-diCH₃O-p-(CH═CHCN)- CN CH₃ H phenyl  50. o,o′-diCH₃O-p-(CH═CHCN)- CN CH₃ benzyl phenyl  51. o,o′-diCH₃O-p-(CH═CHCN)- CN H benzyl phenyl  52. o,o′-diCH₃O-p-(CH═CHCN)- CN H H phenyl  53. o,o′-diCH₃O-p-(CH═CHCN)- CN CH₃ H phenyl  54. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN CH₃ benzyl phenyl  55. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN H benzyl phenyl  56. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN H H phenyl  57. 4-cyclopropylnaphth-1-yl CN CH₃ H  58. 4-cyclopropylnaphth-1-yl CN CH₃ benzyl  59. 4-cyclopropylnaphth-1-yl CN H benzyl  60. 4-cyclopropylnaphth-1-yl CN H H  61. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ H  62. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ benzyl  63. 4-cyclopropylnaphth-1-yl CH═CHCN H benzyl  64. 4-cyclopropylnaphth-1-yl CH═CHCN H H  65. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ H  66. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ benzyl  67. o,o′-di-CH₃O-p-CN-phenyl CN H benzyl  68. o,o′-di-CH₃O-p-CN-phenyl CN H H  69. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ H  70. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ benzyl  71. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H benzyl  72. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H H  73. o,o′-di-CH₃-p-CN-phenyl CN CH₃ H  74. o,o′-di-CH₃-p-CN-phenyl CN CH₃ benzyl  75. o,o′-di-CH₃-p-CN-phenyl CN H benzyl  76. o,o′-di-CH₃-p-CN-phenyl CN H H  77. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ H  78. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ benzyl  79. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H benzyl  80. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H H  81. o,o′-diCH₃O-p-(CH═CHCN)- CN F H phenyl  82. o,o′-diCH₃O-p-(CH═CHCN)- CN F benzyl phenyl  83. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN F benzyl phenyl  84. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN F H phenyl  85. 4-cyclopropylnaphth-1-yl CN F H  86. 4-cyclopropylnaphth-1-yl CN F benzyl  87. 4-cyclopropylnaphth-1-yl CH═CHCN F H  88. 4-cyclopropylnaphth-1-yl CH═CHCN F benzyl  89. o,o′-di-CH₃O-p-CN-phenyl CN F H  90. o,o′-di-CH₃O-p-CN-phenyl CN F benzyl  91. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN F H  92. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN F benzyl  93. o,o′-di-CH₃-p-CN-phenyl CN F H  94. o,o′-di-CH₃-p-CN-phenyl CN F benzyl  95. o,o′-di-CH₃-p-CN-phenyl CH═CHCN F H  96. o,o′-di-CH₃-p-CN-phenyl CH═CHCN F benzyl  97. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ CH₃ H phenyl  98. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ CH₃ benzyl phenyl  99. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ H benzyl phenyl 100. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ H H phenyl 101. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ CH₃ H phenyl 102. o,o′-diCH₃O-p-(CH═CHCN)- F CH₃ benzyl phenyl 103. o,o′-diCH₃O-p-(CH═CHCN)- F H benzyl phenyl 104. o,o′-diCH₃O-p-(CH═CHCN)- F H H phenyl 105. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ H 106. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ benzyl 107. 4-cyclopropylnaphth-1-yl SO₂NH₂ H benzyl 108. 4-cyclopropylnaphth-1-yl SO₂NH₂ H H 109. 4-cyclopropylnaphth-1-yl F CH₃ H 110. 4-cyclopropylnaphth-1-yl F CH₃ benzyl 111. 4-cyclopropylnaphth-1-yl F H benzyl 112. 4-cyclopropylnaphth-1-yl F H H 113. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ H 114. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ benzyl 115. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H benzyl 116. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H H 117. o,o′-di-CH₃O-p-CN-phenyl F CH₃ H 118. o,o′-di-CH₃O-p-CN-phenyl F CH₃ benzyl 119. o,o′-di-CH₃O-p-CN-phenyl F H benzyl 120. o,o′-di-CH₃O-p-CN-phenyl F H H 121. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ H 122. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ benzyl 123. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H benzyl 124. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H H 125. o,o′-di-CH₃-p-CN-phenyl F CH₃ H 126. o,o′-di-CH₃-p-CN-phenyl F CH₃ benzyl 127. o,o′-di-CH₃-p-CN-phenyl F H benzyl 128. o,o′-di-CH₃-p-CN-phenyl F H H 129. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ F H phenyl 130. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ F benzyl phenyl 131. o,o′-diCH₃O-p-(CH═CHCN)- F F benzyl phenyl 132. o,o′-diCH₃O-p-(CH═CHCN)- F F H phenyl 133. 4-cyclopropylnaphth-1-yl SO₂NH₂ F H 134. 4-cyclopropylnaphth-1-yl SO₂NH₂ F benzyl 135. 4-cyclopropylnaphth-1-yl F F H 136. 4-cyclopropylnaphth-1-yl F F benzyl 137. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ F H 138. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ F benzyl 139. o,o′-di-CH₃O-p-CN-phenyl F F H 140. o,o′-di-CH₃O-p-CN-phenyl F F benzyl 141. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ F H 142. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ F benzyl 143. o,o′-di-CH₃-p-CN-phenyl F F H 144. o,o′-di-CH₃-p-CN-phenyl F F benzyl 145. 4-cyclopropyl phenyl CN CH₃ H 146. 4-cyclopropyl phenyl CN CH₃ benzyl 147. 4-cyclopropyl phenyl CN H benzyl 148. 2,4,6-trimethyl phenyl CN H H 149. 2,4,6-trimethyl phenyl CH═CHCN CH₃ H 150. 2,4,6-trimethyl phenyl CH═CHCN CH₃ benzyl 151. 2,4,6-trimethyl phenyl CH═CHCN H benzyl 152. 2,4,6-trimethyl phenyl CH═CHCN H H 153. 2,4,6-trimethyl phenyl CN F H 154. 2,4,6-trimethyl phenyl CN F benzyl 155. 2,4,6-trimethyl phenyl CH═CHCN F H 156. 2,4,6-trimethyl phenyl CH═CHCN F benzyl 157. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ H 158. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ benzyl 159. 2,4,6-trimethyl phenyl SO₂NH₂ H benzyl 160. 2,4,6-trimethyl phenyl SO₂NH₂ H H 161. 2,4,6-trimethyl phenyl F CH₃ H 162. 2,4,6-trimethyl phenyl F CH₃ benzyl 163. 2,4,6-trimethyl phenyl F H benzyl 164. 2,4,6-trimethyl phenyl F H H 165. 2,4,6-trimethyl phenyl SO₂NH₂ F H 166. 2,4,6-trimethyl phenyl SO₂NH₂ F benzyl 167. 4-cyclopropyl phenyl F F H 168. 4-cyclopropyl phenyl F F benzyl 169. 2,4,6-trimethyl phenyl CN CH₃ H 170. 2,4,6-trimethyl phenyl CN CH₃ benzyl 171. 2,4,6-trimethyl phenyl CN H benzyl 172. o,o′-dimethyl-p-cyclopropyl phenyl CN H H 173. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ H 174. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ benzyl 175. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H benzyl 176. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H H 177. o,o′-dimethyl-p-cyclopropyl phenyl CN F H 178. o,o′-dimethyl-p-cyclopropyl phenyl CN F benzyl 179. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN F H 180. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN F benzyl 181. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ H 182. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ benzyl 183. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H benzyl 184. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H H 185. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ H 186. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ benzyl 187. o,o′-dimethyl-p-cyclopropyl phenyl F H benzyl 188. o,o′-dimethyl-p-cyclopropyl phenyl F H H 189. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ F H 190. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ F benzyl 191. 2,4,6-trimethyl phenyl F F H 192. 2,4,6-trimethyl phenyl F F benzyl 193. o,o′-diCH₃O-p-(CH═CHCN)- CN CH₃ CH₃ phenyl 194. o,o′-diCH₃O-p-(CH═CHCN)- CN CH₃ cyclo- phenyl propyl 195. o,o′-diCH₃O-p-(CH═CHCN)- CN H cyclo- phenyl propyl 196. o,o′-diCH₃O-p-(CH═CHCN)- CN H CH₃ phenyl 197. o,o′-diCH₃O-p-(CH═CHCN)- CN CH₃ CH₃ phenyl 198. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN CH₃ cyclo- phenyl propyl 199. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN H cyclo- phenyl propyl 200. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN H CH₃ phenyl 201. 4-cyclopropylnaphth-1-yl CN CH₃ CH₃ 202. 4-cyclopropylnaphth-1-yl CN CH₃ cyclo- propyl 203. 4-cyclopropylnaphth-1-yl CN H cyclo- propyl 204. 4-cyclopropylnaphth-1-yl CN H CH₃ 205. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ CH₃ 206. 4-cyclopropylnaphth-1-yl CH═CHCN CH₃ cyclo- propyl 207. 4-cyclopropylnaphth-1-yl CH═CHCN H cyclo- propyl 208. 4-cyclopropylnaphth-1-yl CH═CHCN H CH₃ 209. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ CH₃ 210. o,o′-di-CH₃O-p-CN-phenyl CN CH₃ cyclo- propyl 211. o,o′-di-CH₃O-p-CN-phenyl CN H cyclo- propyl 212. o,o′-di-CH₃O-p-CN-phenyl CN H CH₃ 213. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ CH₃ 214. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN CH₃ cyclo- propyl 215. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H cyclo- propyl 216. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN H CH₃ 217. o,o′-di-CH₃-p-CN-phenyl CN CH₃ CH₃ 218. o,o′-di-CH₃-p-CN-phenyl CN CH₃ cyclo- propyl 219. o,o′-di-CH₃-p-CN-phenyl CN H cyclo- propyl 220. o,o′-di-CH₃-p-CN-phenyl CN H CH₃ 221. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ CH₃ 222. o,o′-di-CH₃-p-CN-phenyl CH═CHCN CH₃ cyclo- propyl 223. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H cyclo- propyl 224. o,o′-di-CH₃-p-CN-phenyl CH═CHCN H CH₃ 225. o,o′-diCH₃O-p-(CH═CHCN)- CN F CH₃ phenyl 226. o,o′-diCH₃O-p-(CH═CHCN)- CN F cyclo- phenyl propyl 227. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN F cyclo- phenyl propyl 228. o,o′-diCH₃O-p-(CH═CHCN)- CH═CHCN F CH₃ phenyl 229. 4-cyclopropylnaphth-1-yl CN F CH₃ 230. 4-cyclopropylnaphth-1-yl CN F cyclo- propyl 231. 4-cyclopropylnaphth-1-yl CH═CHCN F CH₃ 232. 4-cyclopropylnaphth-1-yl CH═CHCN F cyclo- propyl 233. o,o′-di-CH₃O-p-CN-phenyl CN F CH₃ 234. o,o′-di-CH₃O-p-CN-phenyl CN F cyclo- propyl 235. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN F CH₃ 236. o,o′-di-CH₃O-p-CN-phenyl CH═CHCN F cyclo- propyl 237. o,o′-di-CH₃-p-CN-phenyl CN F CH₃ 238. o,o′-di-CH₃-p-CN-phenyl CN F cyclo- propyl 239. o,o′-di-CH₃-p-CN-phenyl CH═CHCN F CH₃ 240. o,o′-di-CH₃-p-CN-phenyl CH═CHCN F cyclo- propyl 241. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ CH₃ CH₃ phenyl 242. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ CH₃ cyclo- phenyl propyl 243. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ H cyclo- phenyl propyl 244. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ H CH₃ phenyl 245. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ CH₃ CH₃ phenyl 246. o,o′-diCH₃O-p-(CH═CHCN)- F CH₃ cyclo- phenyl propyl 247. o,o′-diCH₃O-p-(CH═CHCN)- F H cyclo- phenyl propyl 248. o,o′-diCH₃O-p-(CH═CHCN)- F H CH₃ phenyl 249. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ CH₃ 250. 4-cyclopropylnaphth-1-yl SO₂NH₂ CH₃ cyclo- propyl 251. 4-cyclopropylnaphth-1-yl SO₂NH₂ H cyclo- propyl 252. 4-cyclopropylnaphth-1-yl SO₂NH₂ H CH₃ 253. 4-cyclopropylnaphth-1-yl F CH₃ CH₃ 254. 4-cyclopropylnaphth-1-yl F CH₃ cyclo- propyl 255. 4-cyclopropylnaphth-1-yl F H cyclo- propyl 256. 4-cyclopropylnaphth-1-yl F H CH₃ 257. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ CH₃ 258. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ CH₃ cyclo- propyl 259. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H cyclo- propyl 260. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ H CH₃ 261. o,o′-di-CH₃O-p-CN-phenyl F CH₃ CH₃ 262. o,o′-di-CH₃O-p-CN-phenyl F CH₃ cyclo- propyl 263. o,o′-di-CH₃O-p-CN-phenyl F H cyclo- propyl 264. o,o′-di-CH₃O-p-CN-phenyl F H CH₃ 265. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ CH₃ 266. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ CH₃ cyclo- propyl 267. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H cyclo- propyl 268. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ H CH₃ 269. o,o′-di-CH₃-p-CN-phenyl F CH₃ CH₃ 270. o,o′-di-CH₃-p-CN-phenyl F CH₃ cyclo- propyl 271. o,o′-di-CH₃-p-CN-phenyl F H cyclo- propyl 272. o,o′-di-CH₃-p-CN-phenyl F H CH₃ 273. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ F CH₃ phenyl 274. o,o′-diCH₃O-p-(CH═CHCN)- SO₂NH₂ F cyclo- phenyl propyl 275. o,o′-diCH₃O-p-(CH═CHCN)- F F cyclo- phenyl propyl 276. o,o′-diCH₃O-p-(CH═CHCN)- F F CH₃ phenyl 277. 4-cyclopropylnaphth-1-yl SO₂NH₂ F CH₃ 278. 4-cyclopropylnaphth-1-yl SO₂NH₂ F cyclo- propyl 279. 4-cyclopropylnaphth-1-yl F F CH₃ 280. 4-cyclopropylnaphth-1-yl F F cyclo- propyl 281. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ F CH₃ 282. o,o′-di-CH₃O-p-CN-phenyl SO₂NH₂ F cyclo- propyl 283. o,o′-di-CH₃O-p-CN-phenyl F F CH₃ 284. o,o′-di-CH₃O-p-CN-phenyl F F cyclo- propyl 285. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ F CH₃ 286. o,o′-di-CH₃-p-CN-phenyl SO₂NH₂ F cyclo- propyl 287. o,o′-di-CH₃-p-CN-phenyl F F CH₃ 288. o,o′-di-CH₃-p-CN-phenyl F F cyclo- propyl 289. 2,4,6-trimethyl phenyl CN CH₃ CH₃ 290. 2,4,6-trimethyl phenyl CN CH₃ cyclo- propyl 291. 2,4,6-trimethyl phenyl CN H cyclo- propyl 292. 2,4,6-trimethyl phenyl CN H CH₃ 293. 2,4,6-trimethyl phenyl CH═CHCN CH₃ CH₃ 294. 2,4,6-trimethyl phenyl CH═CHCN CH₃ cyclo- propyl 295. 2,4,6-trimethyl phenyl CH═CHCN H cyclo- propyl 296. 2,4,6-trimethyl phenyl CH═CHCN H CH₃ 297. 2,4,6-trimethyl phenyl CN F CH₃ 298. 2,4,6-trimethyl phenyl CN F cyclo- propyl 299. 2,4,6-trimethyl phenyl CH═CHCN F CH₃ 300. 2,4,6-trimethyl phenyl CH═CHCN F cyclo- propyl 301. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ CH₃ 302. 2,4,6-trimethyl phenyl SO₂NH₂ CH₃ cyclo- propyl 303. 2,4,6-trimethyl phenyl SO₂NH₂ H cyclo- propyl 304. 2,4,6-trimethyl phenyl SO₂NH₂ H CH₃ 305. 2,4,6-trimethyl phenyl F CH₃ CH₃ 306. 2,4,6-trimethyl phenyl F CH₃ cyclo- propyl 307. 2,4,6-trimethyl phenyl F H cyclo- propyl 308. 2,4,6-trimethyl phenyl F H CH₃ 309. 4-cyclopropyl phenyl SO₂NH₂ F CH₃ 310. 4-cyclopropyl phenyl SO₂NH₂ F cyclo- propyl 311. 4-cyclopropyl phenyl F F CH₃ 312. 4-cyclopropyl phenyl F F cyclo- propyl 313. o,o′-dimethyl-p-cyclopropyl phenyl CN CH₃ CH₃ 314. o,o′-dimethyl-p-cyclopropyl phenyl CN CH₃ cyclo- propyl 315. o,o′-dimethyl-p-cyclopropyl phenyl CN H cyclo- propyl 316. o,o′-dimethyl-p-cyclopropyl phenyl CN H CH₃ 317. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ CH₃ 318. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN CH₃ cyclo- propyl 319. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H cyclo- propyl 320. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN H CH₃ 321. o,o′-dimethyl-p-cyclopropyl phenyl CN F CH₃ 322. o,o′-dimethyl-p-cyclopropyl phenyl CN F cyclo- propyl 323. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN F CH₃ 324. o,o′-dimethyl-p-cyclopropyl phenyl CH═CHCN F cyclo- propyl 325. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ CH₃ 326. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ CH₃ cyclo- propyl 327. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H cyclo- propyl 328. o,o′-dimethyl-p-cyclopropyl phenyl SO₂NH₂ H CH₃ 329. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ CH₃ 330. o,o′-dimethyl-p-cyclopropyl phenyl F CH₃ cyclo- propyl 331. o,o′-dimethyl-p-cyclopropyl phenyl F H cyclo- propyl 332. o,o′-dimethyl-p-cyclopropyl phenyl F H CH₃ 333. 2,4,6-trimethyl phenyl SO₂NH₂ F CH₃ 334. 2,4,6-trimethyl phenyl SO₂NH₂ F cyclo- propyl 335. 2,4,6-trimethyl phenyl F F CH₃ 336. 2,4,6-trimethyl phenyl F F cyclo- propyl 337. o,o′-di-CH₃-p-acetyl-phenyl CN H H 338. o,o′-di-CH₃-p-acetyl-phenyl CN CH₃ H 339. o,o′-di-CH₃-p-acetyl-phenyl CN H Cl 340. o,o′-di-CH₃-p-acetyl-phenyl CN CH₃ Cl Additional contemplated and prophetic examples, which are not exhaustive but merely representative of this invention, are shown below: 

1. A compound of formula

where the dashed line represents a double bond between either A and B or B and D, T′ is O or S; A is NZ; B is ═CH; D is ═CW; Z is H, Br, CH₃, CH₂CH₃, cyclopropyl, or benzyl, the phenyl moiety of said benzyl optionally substituted with one or two groups selected independently from methyl and methoxy; W is H, F, Cl, Br, methyl, ethyl, cyclopropyl, allyl, CH₂CF₃, cyanomethyl, CH₂CH₂CN, CH═CHCN, or benzyl, the phenyl moiety of said benzyl optionally substituted with one or two groups selected independently from methyl and methoxy, V is F, Cl, CN, SO₂CH₃, SO₂NH₂, SO₂NHCH₃, C≡CCH₃, or CH═CHCN; Ar is (a), (b), (c), or (d) below

where the dashed lines in (a) represent optional double bonds; R^(P) is Cl, Br, I, CN, methyl, ethyl, n-propyl, isopropyl, cyclopropylmethyl, C₃-C₆ cycloalkyl, CH═CHCN, acetyl, or NH—C₁-C₆ alkyl, said alkyl and cycloalkyl groups optionally substituted with methyl, methoxy, halogen, or cyano; R⁴, R⁵, and R⁶ are, independently, H, F, Cl, Br, CH₃, CH₂F, CHF₂, CF₃, isopropyl, cyclopropyl, OCH₃, OH, OCF₃, NH₂ and NHCH₃, or R⁶ and R^(P) on adjacent ring atoms, together with the ring atoms to which they are attached, form an additional fused five-membered ring; Q and Q′ are, independently, N or CH; R⁷ is Cl, Br, I, CH₃, CF₃, OCH₃, isopropyl, cyclopropyl, t-butyl, or cyclobutyl; and R⁸, R⁹, R¹⁰ and R¹¹ are each, independently, H or CH₃.
 2. The compound of claim 1, wherein Ar is (a) or (c).
 3. The compound of claim 2, where R⁶ either is H or is in the 2-position.
 4. The compound of claim 1, which is a compound of formula IA-2


5. The compound of claim 4, where Ar is 4-cyclopropyl-, 4-acetyl-, 4-methyl-, 4-bromo-, or 4-cyano-2,6-di-substituted phenyl.
 6. The compound of claim 1, where V is CN, and where W is, H, methyl, F, Cl, Br, or benzyl, Z is, H, methyl, Br, or benzyl.
 7. The compound of claim 3 which is a compound of formula IA-2a:


8. The compound of claim 7, where V is CN or CH═CHCN, R⁶ is methyl, methoxy, or chloro and R⁷ is 6-methyl, or 6-methoxy.
 9. The compound of claim 8, where R^(P) is CN, cyclopropyl, methyl, Br, Cl, CH═CHCN, or acetyl.
 10. The compound of claim 9 where V is CN, W is H, chloro, bromo, methyl, or ethyl and Z is H, methyl, ethyl, or benzyl.
 11. A compound of formula IB

where the dashed line represents a double bond between either A and B or B and D, and where A is NZ; B is ═CH; D is ═CW; Z is H, Br, CH₃, CH₂CH₃, cyclopropyl, or benzyl, the phenyl moiety of said benzyl optionally substituted with methyl or methoxy; W is H, F, Cl, Br, methyl, ethyl, cyclopropyl, allyl, CH₂CF₃, cyanomethyl, CH₂CH₂CN, CH═CHCN, or benzyl, the phenyl moiety of said benzyl optionally substituted with methyl or methoxy; V is F, Cl, CN, SO₂CH₃, SO₂NH₂, SO₂NHCH₃, C≡CCH₃, or CH═CHCN, Ar is (a), (b), or (d) below:

where R^(P) is Cl, Br, I, CN, methyl, ethyl, n-propyl, isopropyl, cyclopropylmethyl, C₃-C₆ cycloalkyl, CH═CHCN, acetyl, or NH—C₁-C₆ alkyl, said alkyl and cycloalkyl groups optionally substituted with methyl, methoxy, halogen, or cyano; R⁴, R⁵, and R⁶ are, independently, H, F, Cl, Br, CH₃, CH₂F, CHF₂, CF₃, isopropyl, cyclopropyl, OCH₃, OH, OCF₃, NH₂ and NHCH₃; Q and Q′ are, independently, N or CH; and R⁸, R⁹, R¹⁰ and R¹¹ are each, independently, H or CH₃.
 12. A compound of formula IB-1

where the dashed line represents a double bond between either A and B or B and D; A is NZ; B is ═CH; D is ═CW; Z is H, Br, CH₃, CH₂CH₃, cyclopropyl, or benzyl, the phenyl moiety of said benzyl optionally substituted with methyl or methoxy, W is H, F, Cl, Br, methyl, ethyl, cyclopropyl, allyl, CH₂CF₃, CH₂CN, CH₂CH₂CN, CH═CHCN, or benzyl, the phenyl moiety of said benzyl optionally substituted with methyl or methoxy, V is F, Cl, CN, SO₂CH₃, SO₂NH₂, SO₂NHCH₃, C≡CCH₃, or CH═CHCN; R^(P) is Cl, Br, I, CN, CH═CHCN, methyl, ethyl, n-propyl, isopropyl, cyclopropylmethyl, C₃-C₆ cycloalkyl, acetyl, and NH—C₃-C₆ alkyl; R⁶ is H, F, Cl, Br, CH₃, CH₂F, CHF₂, CF₃, isopropyl, cyclopropyl, OCH₃, OH, OCF₃, NH₂ and NHCH₃; and R⁷ is Cl, Br, I, CH₃, CF₃, OCH₃, isopropyl, cyclopropyl, t-butyl, or cyclobutyl.
 13. The compound of claim 12, where V is CN or CH═CHCN, R⁶ is 2-methyl, 2-methoxy, or 2-chloro and R⁷ is 6-methyl, or 6-methoxy.
 14. The compound of claim 13, where R^(P) is CN, cyclopropyl, methyl, Br, Cl, CH═CHCN, or acetyl. 